- Open Access
Vaccination with live attenuated simian immunodeficiency virus causes dynamic changes in intestinal CD4+CCR5+ T cells
© Li et al; licensee BioMed Central Ltd. 2011
- Received: 4 November 2010
- Accepted: 3 February 2011
- Published: 3 February 2011
Vaccination with live attenuated SIV can protect against detectable infection with wild-type virus. We have investigated whether target cell depletion contributes to the protection observed. Following vaccination with live attenuated SIV the frequency of intestinal CD4+CCR5+ T cells, an early target of wild-type SIV infection and destruction, was determined at days 3, 7, 10, 21 and 125 post inoculation.
In naive controls, modest frequencies of intestinal CD4+CCR5+ T cells were predominantly found within the LPL TTrM-1 and IEL TTrM-2 subsets. At day 3, LPL and IEL CD4+CCR5+ TEM cells were dramatically increased whilst less differentiated subsets were greatly reduced, consistent with activation-induced maturation. CCR5 expression remained high at day 7, although there was a shift in subset balance from CD4+CCR5+ TEM to less differentiated TTrM-2 cells. This increase in intestinal CD4+CCR5+ T cells preceded the peak of SIV RNA plasma loads measured at day 10. Greater than 65.9% depletion of intestinal CD4+CCR5+ T cells followed at day 10, but overall CD4+ T cell homeostasis was maintained by increased CD4+CCR5- T cells. At days 21 and 125, high numbers of intestinal CD4+CCR5- naive TN cells were detected concurrent with greatly increased CD4+CCR5+ LPL TTrM-2 and IEL TEM cells at day 125, yet SIV RNA plasma loads remained low.
This increase in intestinal CD4+CCR5+ T cells, following vaccination with live attenuated SIV, does not correlate with target cell depletion as a mechanism of protection. Instead, increased intestinal CD4+CCR5+ T cells may correlate with or contribute to the protection conferred by vaccination with live attenuated SIV.
- Simian Immunodeficiency Virus
- CCR5 Expression
- Cynomolgus Macaque
- Simian Immunodeficiency Virus Infection
- Naive Control
Non-human primates (NHP) challenged with simian immunodeficiency virus (SIV) or engineered SIV/HIV-1 chimeras (SHIV) have been used as models to evaluate the efficacy of a wide variety of candidate AIDS vaccine approaches for more than two decades [1–6]. Amongst the vaccine strategies evaluated in NHP models, vaccination with live attenuated SIV/SHIV has proven to be the most effective at providing broad protective immunity against a wide range of SIV and SHIV challenges [7–15]. However, concerns regarding the safety of a live attenuated SIV or HIV vaccine have to date limited further pursuit of this approach as an AIDS vaccine strategy in the clinic [16–20]. Nevertheless, the potency of this vaccine protection has led to further studies in NHP models to provide information on the mechanisms of protective immunity that a safe and effective human vaccine may have to reproduce to be of equal efficacy .
Many groups have attempted to identify robust correlates of protection amongst the adaptive immune responses elicited by live attenuated SIV vaccines. Unfortunately a confusing picture has developed, with different groups reporting either partial, full or no correlation with various measures of adaptive immunity [22–39]. This confusion may have resulted from the range of different NHP models used for these studies: using different vaccines, different challenge viruses and different species of macaque. However, since the efficacy of live attenuated vaccines appears to correlate inversely with the level of attenuation [40, 41] and the most effective vaccines persist and replicate in the host , then it is possible that innate responses may also contribute to the vaccine effect [36, 37]. This would appear to be the case with live attenuated vaccines that have been reported to protect within as little as 3 weeks vaccination when adaptive antiviral immune responses are low or absent .
The gut-associated lymphoid tissue (GALT) constitutes a large immune compartment within the body [44–47] which, compared to other lymphoid compartments, is rich in CD4+ T cells expressing CCR5 [48–50], a preferential co-receptor for HIV and SIV infection [51–53]. Early depletion of intestinal CD4+CCR5+ T cells is now a recognised hallmark of wild-type SIV/HIV infection resulting from the destruction of virus infected target cells [46, 48, 54–57]. It could be hypothesised that if live attenuated SIV vaccines caused a similar loss of CD4+CCR5+ T cells in this compartment, then this depletion of target cells could contribute to the vaccine effect. However, it has been reported that vaccination of rhesus macaques with live attenuated SIV does not cause significant loss of intestinal CD4+ T cells [48, 58]. Moreover, it has recently been reported that vaccination with attenuated SIV causes a transient increase in activated CD4+ memory T cells . Nonetheless, dynamic changes in CCR5 expression within intestinal CD4+ T cell memory subsets were not assessed in detail, nor have these types of studies been performed in models involving cynomolgus macaques.
In the present study, we have characterised the impact on CD4+CCR5+ intestinal T cell memory subsets following inoculation with a potent live nef-attenuated SIV vaccine in the cynomolgus macaque model. These data have revealed that vaccination results in dramatic dynamic changes in key lymphocyte subsets in the intestinal tract that appear to be more consistent with immune activation, likely to induce innate and adaptive responses, than target cell depletion. These changes may contribute not only to the kinetics of vaccine protection, but also to the kinetics of virus replication.
Attenuated SIV virus loads in blood and lymphoid tissues peak at day 10
Attenuated SIV does not cause overt depletion of intestinal CD4+ T cells
Attenuated SIV causes dynamic changes in intestinal CD4+CCR5+ T cells
Attenuated SIV upregulates intestinal CD4+ TCM and TEMcell CCR5 expression
Attenuated SIV differentially modulates intestinal LPL and IEL CD4+ T cells
Live attenuated SIV vaccines provide potent protection, but the detailed properties of this protection appear to vary depending upon the model system studied. In this report, we describe further studies to characterise the mechanism of protection conferred by a minimally nef-deleted attenuated vaccine derived from SIVmac251, called SIVmacC8 , in (Mauritian derived) cynomolgus macaques. Vaccination of cynomolgus macaques with SIVmacC8 protects against infection with virus infected cells as well as cell free virus , develop by 3 weeks  and paradoxically protects against a genetically heterologous virus challenge better (N. Berry personal communication) than a highly vigorous homologous virus challenge . Since we have been unable to identify a mechanism of protection amongst adaptive immune responses that develop following vaccination, either by passive transfer of immune serum  or CD8+ T cell depletion [34, 62], we investigated whether other responses to vaccination may contribute to protection. It is accepted that infection with wild-type SIV rapidly induces a depletion of CD4+CCR5+ memory T cells in the GALT [54–57]. Therefore, we speculated whether a similar effect following vaccination with SIVmacC8 would result in target cell depletion, preventing subsequent virus challenges from infecting the GALT and so preventing a systemic infection from being established. The data indicate that, following inoculation of SIVmacC8, marked dynamic changes in CD4+ T cell populations occur that may not only contribute to the protective effect of vaccination, but could also be instrumental in regulating the kinetics of replication by this virus.
Previous reports of T cell dynamics in the GALT of rhesus macaques, following infection with attenuated SIV, suggested that minimal changes occurred since the total CD4+population remained unaltered [48, 58]. This also appeared to be the case for cynomolgus macaques vaccinated with SIVmacC8. However, more detailed analyses of CD4+CCR5+ memory T cell populations revealed a more dynamic picture of events.
By immunostaining with antibodies to CD3, CD4, CCR5, CD28, CD95 and CCR7 markers, it was possible to define the naive and memory helper T cell compartments in considerable detail. Prior to vaccination with SIVmacC8, the low level of CCR5 expression by CD4+ TEM cells in naive cynomolgus macaques would be anticipated with a lack of activation and proinflammatory Th1 responses [63–65]. By contrast, within 3 days of vaccination when the primary viraemia is first detectable, a dramatic expansion of intestinal CD4+CCR5+ TEM cells was detected, consistent with an acute Th1 proinflammatory response [66–68]. This expansion of intestinal CD4+CCR5+ TEM cells was probably a result of activation-associated upregulation of CCR5 expression by CD4+CCR5- T cells, since concurrent reductions in less differentiated CD4+ TCM, TTrM-1 and TTrM-2 cells were detected. Alternative explanations such as the proliferation of intestinal CD4+CCR5+ TEM cells or an influx of CD4+CCR5+ TEM cells into the intestinal mucosa are less likely because of the limited proliferative potential of TEM cells  or the need for co-ordinated outflow of CD4+CCR5- T cells to balance overall CD4+ T cell percentages.
The marked expansion in the activated intestinal CD4+CCR5+ cell population in the absence of acquired immune responses would provide large numbers of target cells in which SIVmacC8 could replicate readily. Indeed, virus infected cells are detectable in the small intestine from day 3 by immunohistochemistry (D. Ferguson personal communication). However, it is not known whether this series of events reflects SIV exploiting a generic host response to infection or whether it is a result of specific viral factors driving events. Nevertheless, not only did the early expansion of intestinal CD4+CCR5+ T cells, detectable from day 3, appear to "fuel" the increases in plasma SIV RNA loads at days 3 and 7, but also the loss of LPL and IEL CD4+CCR5+ TEM cells from day 7 also augured the end of the primary viraemia from day 10 when there were dramatic reductions in remaining LPL and IEL CD4+CCR5+ TTrM-2 cells to pre-infection levels. These data, which were virtually indistinguishable from those previously reported for this virus , suggest that the kinetics of SIVmacC8 primary viraemia may be regulated by the availability of target cells as much as the development of anti-viral immune responses. Studies of the infection of Chinese rhesus macaques with pathogenic SIV have also reported that peak plasma SIV RNA loads were associated with the loss of intestinal CD4+CCR5+ T cells [71, 72]. Nevertheless there is considerable evidence that acquired anti-SIV immune responses, such as CD8+ cytotoxic T cells, regulate viral loads [33, 34, 73–76]. Intriguingly, in a previous report of the primary viraemia of SIVmacC8 during profound CD8+ cell depletion, whilst the peak SIV RNA loads were approximately 300 times higher in the absence of CD8+ T cells, SIV RNA loads declined prior to recovery of detectable CD8+ T cells , indicating that other mechanisms must also contribute to the control of the primary viraemia.
The dramatic loss of intestinal CD4+CCR5+ T cells between days 7 and 10, post vaccination with attenuated SIV, may be due to indirect mechanisms such as CD95 dependant apoptosis  as well as direct lytic viral replication. However, it is unclear why overall CD4+ T cell percentages were not then reduced, as per wild-type SIV infection [48, 58]. It may be that lower cell-associated virus loads and the non-pathogenic nature of attenuated SIV infection reduce rates of CD4+CCR5+ T cell attrition thereby allowing T cell homeostatic repopulation of the GALT to be sustained. Such repopulation could originate from outside the GALT or through expansion of intestinal CD4+CCR5- TEM and TTrM-2 cell populations. Though at this time there were few naive TN cells detectable to suggest repopulation, and TEM cells have been reported to have limited proliferative capacity [77, 78]; however, the high proliferative capacity of CD4+ TTrM-2  cells could have been able to support that repopulation. Alternatively, down regulation of CCR5 expression on CD4+CCR5+ T cells may better account for the dynamic changes observed between days 7 and 10, that is not necessarily due to depletion. In order to address this possibility we need to investigate whether CD4+CCR5- cells harbour attenuated SIV, as others have found with pathogenic SIV .
Nevertheless, at days 21 and 125, there was a dramatic increase in intestinal TN cells that may signify an influx of repopulating cells to replace ongoing losses and maintain homeostasis, as has been reported following infection with pathogenic SIV . Since the second dramatic increase in CD4+CCR5+ intestinal T cells at day 125 occurred without the appearance of increased SIV RNA loads, other factors not present during the acute infection must be restricting SIV replication, preventing further loss of intestinal CD4+CCR5+ T cells. Further work is needed to determine whether adaptive immune or other anti-viral responses, such as retroviral superinfection resistance, are involved at these later times specifically . Whatever the mechanism identified, it needs to be able to account for the characterised properties of protection conferred by live attenuated vaccines in the species of macaque being studied.
One of the difficulties for understanding vaccine protection conferred by live attenuated SIV has been the frequently confusing, if not conflicting data, obtained by different groups using related vaccine models but in different species of macaque. In this report, we found a much lower frequencies of intestinal CD4+CCR5+ T cells (16.16% ± 2.44%) in naive cynomolgus macaques compared with Indian rhesus macaques, where the level of CCR5 expression by CD4+ intestinal T cells is reported to be >60% . Intriguingly, average levels of CCR5 expression on CD4+ intestinal T cells of SIV natural hosts is reported to be considerably lower those we have described. For example, 9.13% for African green monkeys and 1.2% for sooty mangabeys . It may be hypothesised that this lower level of CCR5 expression by CD4+ T cells may contribute to the more limited damage of the immune system caused by wild-type SIV in these hosts as there would be reduced numbers of target cells susceptible to infection and destruction at any time . Conversely, the higher levels of CCR5 expression on peripheral CD4+ T cells of Indian versus Chinese rhesus macaques, 21.8% ± 7.7% and 6.7% ± 4.6% respectively, could contribute to the sustained high virus load and faster disease progression seen in Indian rhesus macaques infected with SIV [72, 81]. If alterations in the frequency of these same CD4+ T cell subsets contribute not only to viral kinetics but also to the protection mediated by live attenuated SIV, then it may be anticipated that undertaking a similar vaccine study in macaques of different species could result in distinct outcomes.
Vaccination with live attenuated SIV causes dynamic changes and chronic expansion of CD4+CCR5+ intestinal T cell memory subsets, more consistent with immune activation than target cell depletion. The profile of high frequencies of CD4+CCR5+ T cells detectable in the GALT after vaccination is not identical to those found in naive animals or expanded during the early stages of the primary viraemia, implying lasting immune modulation. Understanding the impact of the immune modulation caused by attenuated SIV and the mechanism(s) involved may provide insight into the development of novel vaccine approaches or therapies that safely reproduce this protection.
In this study, twenty D-type-retrovirus-free juvenile cynomolgus macaques (Macaca fascicularis), housed and maintained in accordance with UK Home Office guidelines for the care and maintenance of nonhuman primates, were used. Animals were sedated with ketamine hydrochloride before inoculation of virus or venepuncture and killed humanely by an overdose of anaesthetic. The vaccine virus SIVmacC8 is a clone of a rhesus passage of wild-type SIVmac251  attenuated by a 12 bp in-frame deletion in the nef open reading frame and two further conservative amino acid changes . Cynomolgus macaques were inoculated with vaccine virus by intravenous injection of 5000 TCID50 of the 9/90 pool of SIVmacC8 , which has an end-point titre of 104 TCID50/ml on C8166 cells, and were sacrificed in pairs on days 3, 7, 10, 21 and 125 (n = 2) in the first study and days 3, 10 and 21 (n = 2) in a second study for analysis and comparison with naive macaques (n = 4) of CCR5 expression across CD4+ T cell memory subsets.
PBMCs were isolated by density gradient centrifugation as previously described . Spleen, PLN and MLN cells were isolated by mechanical tissue disaggregation (Medimachine, BD Biosciences, Oxford, UK). LPL and IEL were isolated from the SI and LI. Briefly, intestinal sections were opened longitudinally, cut into 5 cm segments and washed with cold HBSS (Gibco®Invitrogen Ltd., Paisley, UK). Segments were then incubated in cold Ca2+ and Mg2+ free HBSS (Gibco®Invitrogen Ltd., Paisley, UK) containing 10 mM Dithiothreitol (Sigma-Aldrich, Dorset, UK) on an orbital shaker for 45-60 minutes at 4°C. After incubation IEL were collected as the filtrate from a 100 μm cell strainer (BD Biosciences, Oxford, UK). Remaining intestinal tissue was then incubated with warm collagenase solution (0.5 mg/ml) on an orbital shaker at 37°C for 30-45 minutes. After incubation LPL were collected as the filtrate from a 100 μm cell strainer (BD Biosciences, Oxford, UK). All extracted filtrates were centrifuged at 400 g for 10 min, pellets re-suspended in RPMI 1640 (Sigma-Aldrich, Dorset, UK), layered onto FCS and spun at 400 g for 10 min. Cell pellets were re-suspended in RPMI 1640 containing 2 mg/ml DNAse (Sigma-Aldrich, Dorset, UK) and incubated for 20 min on shaker at 37°C. Cell suspensions were layered over a 35% Percoll gradient (Sigma-Aldrich, Dorset, UK) which was layered over a 65% Percoll gradient and centrifuged at 500 g for 30 min. Lymphocytes present at the interface between the 35% and 65% Percoll layers were aspirated and cells washed twice in RPMI 1640. Prior to staining cells were further processed using a "Dead Cell Removal Kit", according to manufacturer's instructions, to reduce debris (Miltenyi Biotec, Surrey, UK).
Detection and quantification of SIV RNA, DNA and cell-associated virus
SIV RNA levels in plasma were determined by quantitative real-time RT-PCR (qRT-PCR) as previously described . Viral RNA was extracted from 140 μl plasma using viral RNA mini-kits (QIAamp; Qiagen, Crawley, UK) then eluted in a total volume of 50 μl AVE buffer. RNA (5 μl) extracted from reference or experimental samples were amplified in triplicate using the Brilliant QRT-PCR plus Core Reagents one-step kit (Agilent Technologies Inc., CA, USA). Oligonucleotide primers and probe sequences, located in conserved regions of gag, were optimized at 300 and 100 nM respectively . A value of 1.3 log10 SIV RNA copies per ml is below the cut-off for quantification in this assay. Cell-associated virus loads of isolated lymphoid cells were determined by co-culture with C8166 cells, and the presence of replicating virus was confirmed by syncytia identification or by antigen capture at 28 days .
Genomic DNA was extracted from 106 purified intestinal lymphocytes (as described above) and proviral SIV gag DNA levels determined by quantitative PCR (qPCR), using the same primer/probe sequences as the qRT-PCR assay . The concentration added to each PCR assay was determined retrospectively using a fluorometic DNA quantification kit (Sigma-Aldrich, Dorset, UK) in a microtitre format. Aliquots of DNA (1 μl) were assayed in triplicate using a Taqman Universal PCR Master Mix (ABI) against a standard curve of the p2-LTR plasmid  serially diluted in herring sperm DNA . SIV DNA levels were expressed as copies of SIV DNA per 105 mononuclear cells (MNC) with an absolute limit of detection being 1 SIV DNA copy per 105 cells.
Analysis of CCR5 expression by T cell memory subsets
Expression of CCR5 within T cell subsets defined by CD3-FITC (clone FN18, AbD Serotec, UK), CD4-APC-Cy7 (clone OKT4, Biolegend, Cambridge, UK), CD8-AmCyan (clone SK1, BD Biosciences, Oxford, UK), CD28-PerCP-Cy5.5 (clone CD28.2, eBioscience Ltd., Hatfield, UK), CD95-PE-Cy7 (clone DX2, eBioscience Ltd., Hatfield, UK) and CCR7-FITC (clone 150503, R&D systems, Abingdon, UK) was assessed by flow cytometry. Within the CD3+CD4+ (helper) T cell subset, naive (CD95-CD28+, TN), central memory (CD95+CD28+ or CD95+CD28+CCR7+CCR5-, TCM), transitional memory subset-1 (CD95+CD28+CCR7+CCR5+, TTrM-1), transitional memory subset-2 (CD95+CD28+CCR7-, TTrM-2) and effector memory (CD95+CD28- or CD95+CD28-CCR7-, TEM) distinctions were made [59, 60]. Staining was performed as previously described . Acquisition was performed using a BD FACSCanto II and analysed using BD FACSDiva software (BD Biosciences, Oxford, UK). At least 10,000 CD3+CD4+ events were collected for subset analysis.
Immunohistochemical analysis was performed as previously described . Briefly formaldehyde fixed, paraffin embedded tissue sections were de-waxed, and re-hydrated before being incubated with 50 μg/ml proteinase K (Roche Products Ltd., Welwyn Garden City, UK) in PBS pH7.4 for 15 minutes at 37°C to unmask target antigens followed by immuno-labelling with anti-CCR5 (3A9, BD Biosciences, Oxford, UK). Bound antibodies were visualized using the Vector ABC amplification system (Vector Laboratories, Peterborough, UK) in combination with a biotinylated universal anti-mouse/rabbit secondary antibody (Vector Laboratories, Peterborough, UK).
A Kruskal-Wallis test followed by Dunn's post test was used for comparison of CD3+CD4+ and CD3+CD4+CCR5+ counts and plasma SIV vRNA loads at each time point measured. Values expressed are mean ± standard error of means (SEM). All reported P values were two sided at the 0.05 significance level determined using Prism 5 software (Graph Pad Software, CA, USA).
We thank the technical and veterinary staff at NIBSC for animal care. This work was funded by MRC grant G0600007.
- Desrosiers RC, Wyand MS, Kodama T, Ringler DJ, Arthur LO, Sehgal PK, Letvin NL, King NW, Daniel MD: Vaccine protection against simian immunodeficiency virus infection. Proc Natl Acad Sci USA. 1989, 86: 6353-6357. 10.1073/pnas.86.16.6353.PubMed CentralView ArticlePubMedGoogle Scholar
- Hu SL, Zarling JM, Chinn J, Travis BM, Moran PA, Sias J, Kuller L, Morton WR, Heidecker G, Benveniste RE: Protection of macaques against simian AIDS by immunization with a recombinant vaccinia virus expressing the envelope glycoproteins of simian type D retrovirus. Proc Natl Acad Sci USA. 1989, 86: 7213-7217. 10.1073/pnas.86.18.7213.PubMed CentralView ArticlePubMedGoogle Scholar
- Stott EJ, Almond N, Kent K, Walker B, Hull R, Rose J, Silvera P, Sangster R, Corcoran T, Lines J, Silvera K, Luciw P, Murphy-Corb M, Momin P, Bruck C: Evaluation of a candidate human immunodeficiency virus type 1 (HIV-1) vaccine in macaques: effect of vaccination with HIV-1 gp120 on subsequent challenge with heterologous simian immunodeficiency virus-HIV-1 chimeric virus. J Gen Virol. 1998, 79: 423-432.View ArticlePubMedGoogle Scholar
- Hanke T, Samuel RV, Blanchard TJ, Neumann VC, Allen TM, Boyson JE, Sharpe SA, Cook N, Smith GL, Watkins DI, Cranage MP, McMichael AJ: Effective induction of simian immunodeficiency virus-specific cytotoxic T lymphocytes in macaques by using a multiepitope gene and DNA prime-modified vaccinia virus Ankara boost vaccination regimen. J Virol. 1999, 73: 7524-7532.PubMed CentralPubMedGoogle Scholar
- Berry N, Stebbings R, Brown S, Christian P, Thorstensson R, Ahmed RK, Davis L, Ferguson D, D'Arcy N, Elsley W, Hull R, Lines J, Wade-Evans A, Stott J, Almond N: Immunological responses and viral modulatory effects of vaccination with recombinant modified vaccinia virus Ankara (rMVA) expressing structural and regulatory transgenes of simian immunodeficiency virus (SIVmac32H/J5M). J Med Primatol. 2007, 36: 80-94. 10.1111/j.1600-0684.2007.00216.x.View ArticlePubMedGoogle Scholar
- Barnett SW, Burke B, Sun Y, Kan E, Legg H, Lian Y, Bost K, Zhou F, Goodsell A, Zur Megede J, Polo J, Donnelly J, Ulmer J, Otten GR, Miller CJ, Vajdy M, Srivastava IK: Antibody-mediated protection against mucosal simian-human immunodeficiency virus challenge of macaques immunized with alphavirus replicon particles and boosted with trimeric envelope glycoprotein in MF59 adjuvant. J Virol. 2010, 84: 5975-5985. 10.1128/JVI.02533-09.PubMed CentralView ArticlePubMedGoogle Scholar
- Daniel MD, Kirchhoff F, Czajak SC, Sehgal PK, Desrosiers RC: Protective effects of a live attenuated SIV vaccine with a deletion in the nef gene. Science. 1992, 258: 1938-1941. 10.1126/science.1470917.View ArticlePubMedGoogle Scholar
- Almond N, Kent K, Cranage M, Rud E, Clarke B, Stott EJ: Protection by attenuated simian immunodeficiency virus in macaques against challenge with virus-infected cells. Lancet. 1995, 345: 1342-1344. 10.1016/S0140-6736(95)92540-6.View ArticlePubMedGoogle Scholar
- Bogers WM, Niphuis H, Ten Haaft P, Laman JD, Koornstra W, Heeney JL: Protection from HIV-1 envelope-bearing chimeric simian immunodeficiency virus (SHIV) in rhesus macaques infected with attenuated SIV: consequences of challenge. AIDS. 1995, 9: F13-F18.PubMedGoogle Scholar
- Dunn CS, Hurtrel B, Beyer C, Gloeckler L, Ledger TN, Moog C, Kieny MP, Mehtali M, Schmitt D, Gut JP, Kirn A, Aubertin AM: Pathogenicity of live, attenuated SIV after mucosal infection of neonatal macaques.Google Scholar
- Shibata R, Siemon C, Czajak SC, Desrosiers RC, Martin MA : Live, attenuated simian immunodeficiency virus vaccines elicit potent resistance against a challenge with a human immunodeficiency virus type 1 chimeric virus. J Virol. 1997, 71: 8141-8148.PubMed CentralPubMedGoogle Scholar
- Nilsson C, Mäkitalo B, Thorstensson R, Norley S, Binninger-Schinzel D, Cranage M, Rud E, Biberfeld G, Putkonen P: Live attenuated simian immunodeficiency virus (SIV)mac in macaques can induce protection against mucosal infection with SIVsm. AIDS. 1998, 12: 2261-2270. 10.1097/00002030-199817000-00006.View ArticlePubMedGoogle Scholar
- Wyand MS, Manson K, Montefiori DC, Lifson JD, Johnson RP, Desrosiers RC: Protection by live, attenuated simian immunodeficiency virus against heterologous challenge. J Virol. 1999, 73: 8356-8363.PubMed CentralPubMedGoogle Scholar
- Kumar A, Mukherjee S, Shen J, Buch S, Li Z, Adany I, Liu Z, Zhuge W, Piatak M, Lifson J, McClure H, Narayan O: Immunization of macaques with live simian human immunodeficiency virus (SHIV) vaccines conferred protection against AIDS induced by homologous and heterologous SHIVs and simian immunodeficiency virus. Virology. 2002, 301: 189-205. 10.1006/viro.2002.1544.View ArticlePubMedGoogle Scholar
- Reynolds MR, Weiler AM, Weisgrau KL, Piaskowski SM, Furlott JR, Weinfurter JT, Kaizu M, Soma T, León EJ, MacNair C, Leaman DP, Zwick MB, Gostick E, Musani SK, Price DA, Friedrich TC, Rakasz EG, Wilson NA, McDermott AB, Boyle R, Allison DB, Burton DR, Koff WC, Watkins DI: Macaques vaccinated with live-attenuated SIV control replication of heterologous virus. J Exp Med. 2008, 205: 2537-2550. 10.1084/jem.20081524.PubMed CentralView ArticlePubMedGoogle Scholar
- Baba TW, Jeong YS, Pennick D, Bronson R, Greene MF, Ruprecht RM: Pathogenicity of live, attenuated SIV after mucosal infection of neonatal macaques. Science. 1995, 267: 1820-1825. 10.1126/science.7892606.View ArticlePubMedGoogle Scholar
- Whatmore AM, Cook N, Hall GA, Sharpe S, Rud EW, Cranage MP: Repair and evolution of nef in vivo modulates simian immunodeficiency virus virulence. J Virol. 1995, 69: 5117-5123.PubMed CentralPubMedGoogle Scholar
- Learmont JC, Geczy AF, Mills J, Ashton LJ, Raynes-Greenow CH, Garsia RJ, Dyer WB, McIntyre L, Oelrichs RB, Rhodes DI, Deacon NJ, Sullivan JS: Immunologic and virologic status after 14 to 18 years of infection with an attenuated strain of HIV-1. A report from the Sydney Blood Bank Cohort. N Engl J Med. 1999, 340: 1715-1722. 10.1056/NEJM199906033402203.View ArticlePubMedGoogle Scholar
- Sawai ET, Hamza MS, Ye M, Shaw KE, Luciw PA: Pathogenic conversion of live attenuated simian immunodeficiency virus vaccines is associated with expression of truncated Nef. J Virol. 2000, 74: 2038-2045. 10.1128/JVI.74.4.2038-2045.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Hofmann-Lehmann R, Vlasak J, Williams AL, Chenine AL, McClure HM, Anderson DC, O'Neil S, Ruprecht RM: Live attenuated, nef-deleted SIV is pathogenic in most adult macaques after prolonged observation. AIDS. 2003, 17: 157-166. 10.1097/00002030-200301240-00004.View ArticlePubMedGoogle Scholar
- Friedrich TC, Watkins DI: Wanted: correlates of vaccine-induced protection against simian immunodeficiency virus. Curr Opin HIV AIDS. 2008, 3: 393-398. 10.1097/COH.0b013e3282faa461.View ArticlePubMedGoogle Scholar
- Stahl-Hennig C, Dittmer U, Nisslein T, Pekrun K, Petry H, Jurkiewicz E, Fuchs D, Wachter H, Rud EW, Hunsmann G: Attenuated SIV imparts immunity to challenge with pathogenic spleen-derived SIV but cannot prevent repair of the nef deletion. Immunol Lett. 1996, 51: 129-135. 10.1016/0165-2478(96)02567-9.View ArticlePubMedGoogle Scholar
- Wyand MS, Manson KH, Garcia-Moll M, Montefiori D, Desrosiers RC: Vaccine protection by a triple deletion mutant of simian immunodeficiency virus. J Virol. 1996, 70: 3724-3733.PubMed CentralPubMedGoogle Scholar
- Almond N, Rose J, Sangster R, Silvera P, Stebbings R, Walker B, Stott EJ: Mechanisms of protection induced by attenuated simian immunodeficiency virus. I. Protection cannot be transferred with immune serum. J Gen Virol. 1997, 78: 1919-1922.View ArticlePubMedGoogle Scholar
- Connor RI, Montefiori DC, Binley JM, Moore JP, Bonhoeffer S, Gettie A, Fenamore EA, Sheridan KE, Ho DD, Dailey PJ, Marx PA: Temporal analyses of virus replication, immune responses, and efficacy in rhesus macaques immunized with a live, attenuated simian immunodeficiency virus vaccine. J Virol. 1998, 72: 7501-7509.PubMed CentralPubMedGoogle Scholar
- Langlois AJ, Desrosiers RC, Lewis MG, KewalRamani VN, Littman DR, Zhou JY, Manson K, Wyand MS, Bolognesi DP, Montefiori DC: Neutralizing antibodies in sera from macaques immunized with attenuated simian immunodeficiency virus. J Virol. 1998, 72: 6950-6955.PubMed CentralPubMedGoogle Scholar
- Nixon DF, Donahoe SM, Kakimoto WM, Samuel RV, Metzner KJ, Gettie A, Hanke T, Marx PA, Connor RI: Simian immunodeficiency virus-specific cytotoxic T lymphocytes and protection against challenge in rhesus macaques immunized with a live attenuated simian immunodeficiency virus vaccine. Virology. 2000, 266: 203-210. 10.1006/viro.1999.0078.View ArticlePubMedGoogle Scholar
- Johnson RP: Mechanisms of protection against simian immunodeficiency virus infection. Vaccine. 2002, 20: 1985-1987. 10.1016/S0264-410X(02)00083-X.View ArticlePubMedGoogle Scholar
- Almond NM, Stott EJ, Berry N, Wade-Evans AM, Hull R, Lines J, Silvera P, Sangster R, Corcoran T, Rose J, Walker KB: Mechanisms of protection induced by attenuated simian immunodeficiency virus. Virology. 2002, 296: 338-353. 10.1006/viro.2002.1379.View ArticlePubMedGoogle Scholar
- Abel K, Compton L, Rourke T, Montefiori D, Lu D, Rothaeusler K, Fritts L, Bost K, Miller CJ: Simian-human immunodeficiency virus SHIV89.6-induced protection against intravaginal challenge with pathogenic SIVmac239 is independent of the route of immunization and is associated with a combination of cytotoxic T-lymphocyte and alpha interferon responses. J Virol. 2003, 77: 3099-3118. 10.1128/JVI.77.5.3099-3118.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Sharpe SA, Cope A, Dowall S, Berry N, Ham C, Heeney JL, Hopkins D, Easterbrook L, Dennis M, Almond N, Cranage M: Macaques infected long-term with attenuated simian immunodeficiency virus (SIVmac) remain resistant to wild-type challenge, despite declining cytotoxic T lymphocyte responses to an immunodominant epitope. J Gen Virol. 2004, 85: 2591-2602. 10.1099/vir.0.80050-0.View ArticlePubMedGoogle Scholar
- Tenner-Racz K, Stahl Hennig C, Uberla K, Stoiber H, Ignatius R, Heeney J, Steinman RM, Racz P: Early protection against pathogenic virus infection at a mucosal challenge site after vaccination with attenuated simian immunodeficiency virus. Proc Natl Acad Sci USA. 2004, 101: 3017-3022. 10.1073/pnas.0308677101.PubMed CentralView ArticlePubMedGoogle Scholar
- Schmitz JE, Johnson RP, McClure HM, Manson KH, Wyand MS, Kuroda MJ, Lifton MA, Khunkhun RS, McEvers KJ, Gillis J, Piatak M, Lifson JD, Grosschupff G, Racz P, Tenner-Racz K, Rieber EP, Kuus-Reichel K, Gelman RS, Letvin NL, Montefiori DC, Ruprecht RM, Desrosiers RC, Reimann KA: Effect of CD8+ lymphocyte depletion on virus containment after simian immunodeficiency virus SIVmac251 challenge of live attenuated SIVmac239delta3-vaccinated rhesus macaques. J Virol. 2005, 79: 8131-8141. 10.1128/JVI.79.13.8131-8141.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Stebbings R, Berry N, Waldmann H, Bird P, Hale G, Stott J, North D, Hull R, Hall J, Lines J, Brown S, D'Arcy N, Davis L, Elsley W, Edwards C, Ferguson D, Allen J, Almond N: CD8+ lymphocytes do not mediate protection against acute superinfection 20 days after vaccination with a live attenuated simian immunodeficiency virus. J Virol. 2005, 79: 12264-122672. 10.1128/JVI.79.19.12264-12272.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Gauduin MC, Yu Y, Barabasz A, Carville A, Piatak M, Lifson JD, Desrosiers RC, Johnson RP : Induction of a virus-specific effector-memory CD4+ T cell response by attenuated SIV infection. J Exp Med. 2006, 203: 2661-2672. 10.1084/jem.20060134.PubMed CentralView ArticlePubMedGoogle Scholar
- Goletti D, Macchia I, Leone P, Pace M, Sernicola L, Pavone-Cossut MR, Maggiorella MT, Cafaro A, Ensoli B, Titti F: Innate anti-viral immunity is associated with the protection elicited by the simian immunodeficiency virus (SIV) live attenuated virus vaccine in cynomolgus monkeys. Med Sci Monit. 2006, 12: BR330-BR340.PubMedGoogle Scholar
- Berry N, Stebbings R, Ferguson D, Ham C, Alden J, Brown S, Jenkins A, Lines J, Duffy L, Davis L, Elsley W, Page M, Hull R, Stott J, Almond N: Resistance to superinfection by a vigorously replicating, uncloned stock of simian immunodeficiency virus (SIVmac251) stimulates replication of a live attenuated virus vaccine (SIVmacC8). J Gen Virol. 2008, 89: 2240-2251. 10.1099/vir.0.2008/001693-0.View ArticlePubMedGoogle Scholar
- Salha MD, Cheynier R, Halwani R, McGrath H, Langaee TY, Yassine Diab B, Fournier J, Parenteau M, Edgar J, Ko D, Sherring A, Bogdanovic D, Sekaly RP, Rud EW: Persistence of restricted CD4 T cell expansions in SIV-infected macaques resistant to SHIV89.6P superinfection. Virology. 2008, 377: 239-247. 10.1016/j.virol.2008.04.031.PubMed CentralView ArticlePubMedGoogle Scholar
- Mansfield K, Lang SM, Gauduin MC, Sanford HB, Lifson JD, Johnson RP, Desrosiers RC: Vaccine protection by live, attenuated simian immunodeficiency virus in the absence of high-titer antibody responses and high-frequency cellular immune responses measurable in the periphery. J Virol. 2008, 82: 4135-4148. 10.1128/JVI.00015-08.PubMed CentralView ArticlePubMedGoogle Scholar
- Johnson RP, Lifson JD, Czajak SC, Cole KS, Manson KH, Glickman R, Yang J, Montefiori DC, Montelaro R, Wyand MS, Desrosiers RC: Highly attenuated vaccine strains of simian immunodeficiency virus protect against vaginal challenge: inverse relationship of degree of protection with level of attenuation. J Virol. 1999, 73: 4952-4961.PubMed CentralPubMedGoogle Scholar
- van der Kuyl AC, Kozaczynska K, Arien KK, Gali Y, Balazs VR, Dekker SJ, Zorgdrager F, Vanham G, Berkhout B, Cornelissen M: Analysis of infectious virus clones from two HIV-1 superinfection cases suggests that the primary strains have lower fitness. Retrovirology. 2010, 7: 60-74. 10.1186/1742-4690-7-60.PubMed CentralView ArticlePubMedGoogle Scholar
- Denesvre C, Le Grand R, Boissin-Cans F, Chakrabarti L, Hurtrel B, Vaslin B, Dormont D, Sonigo P: Highly attenuated SIVmac142 is immunogenic but does not protect against SIVmac251 challenge. AIDS Res Hum Retroviruses. 1995, 11: 1397-1406. 10.1089/aid.1995.11.1397.View ArticlePubMedGoogle Scholar
- Berry N, Stott J, Hull R, Walker B, Lines J, Elsley W, Brown S, Wade-Evans A, Davis G, Cowie J, Sethi M, Almond N: Vaccination with live attenuated simian immunodeficiency virus for 21 days protects against superinfection. Virology. 2004, 330: 249-260. 10.1016/j.virol.2004.09.026.View ArticlePubMedGoogle Scholar
- Guy-Grand D, Vassalli P: Gut intraepithelial T lymphocytes. Curr Opin Immunol. 1993, 5: 247-252. 10.1016/0952-7915(93)90012-H.View ArticlePubMedGoogle Scholar
- Viney JL: The anatomical basis of intestinal immunity. Immunol Rev. 1997, 156: 145-66. 10.1111/j.1600-065X.1997.tb00966.x.View ArticlePubMedGoogle Scholar
- Smit-McBride Z, Mattapallil JJ, McChesney M, Ferrick D, Dandekar S: Gastrointestinal T lymphocytes retain high potential for cytokine responses but have severe CD4(+) T-cell depletion at all stages of simian immunodeficiency virus infection compared to peripheral lymphocytes. J Virol. 1998, 72: 6646-6656.PubMed CentralPubMedGoogle Scholar
- Ganusov VV, De Boer RJ: Do most lymphocytes in humans really reside in the gut?. Trends Immunol. 2007, 28: 514-518. 10.1016/j.it.2007.08.009.View ArticlePubMedGoogle Scholar
- Veazey RS, Lackner AA: The gastrointestinal tract and the pathogenesis of AIDS. AIDS. 1998, 12 (Suppl A)): S35-S42.PubMedGoogle Scholar
- Agace WW, Roberts AI, Wu L, Greineder C, Ebert EC, Parker CM: Human intestinal lamina propria and intraepithelial lymphocytes express receptors specific for chemokines induced by inflammation. Eur J Immunol. 2000, 30: 819-826. 10.1002/1521-4141(200003)30:3<819::AID-IMMU819>3.0.CO;2-Y.View ArticlePubMedGoogle Scholar
- Anton PA, Elliott J, Poles MA, McGowan IM, Matud J, Hultin LE, Grovit-Ferbas K, Mackay CR, Chen ISY, Giorgi JV: Enhanced levels of functional HIV-1 co-receptors on human mucosal T cells demonstrated using intestinal biopsy tissue. AIDS. 2000, 14: 1761-1765. 10.1097/00002030-200008180-00011.View ArticlePubMedGoogle Scholar
- Chen Z, Gettie A, Ho DD, Marx PA: Primary SIVsm isolates use the CCR5 coreceptor from sooty mangabeys naturally infected in west Africa: a comparison of coreceptor usage of primary SIVsm, HIV-2, and SIVmac. Virology. 1998, 246: 113-124. 10.1006/viro.1998.9174.View ArticlePubMedGoogle Scholar
- Zhang Y, Lou B, Lal RB, Gettie A, Marx PA, Moore JP: Use of inhibitors to evaluate coreceptor usage by simian and simian/human immunodeficiency viruses and human immunodeficiency virus type 2 in primary cells. J Virol. 2000, 74: 6893-68910. 10.1128/JVI.74.15.6893-6910.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Moore JP, Kitchen SG, Pugach P, Zack JA: The CCR5 and CXCR4 coreceptors--central to understanding the transmission and pathogenesis of human immunodeficiency virus type 1 infection. AIDS Res Hum Retroviruses. 2004, 20: 111-126. 10.1089/088922204322749567.View ArticlePubMedGoogle Scholar
- Brenchley JM, Schacker TW, Ruff LE, Price DA, Taylor JH, Beilman GJ, Nguyen PL, Khoruts A, Larson M, Haase AT, Douek DC: CD4+ T cell depletion during all stages of HIV disease occurs predominantly in the gastrointestinal tract. J Exp Med. 2004, 200: 749-759. 10.1084/jem.20040874.PubMed CentralView ArticlePubMedGoogle Scholar
- Mehandru S, Poles MA, Tenner-Racz K, Horowitz A, Hurley A, Hogan C, Boden D, Racz P, Markowitz M: Primary HIV-1 infection is associated with preferential depletion of CD4+ T lymphocytes from effector sites in the gastrointestinal tract. J Exp Med. 2004, 200: 761-770. 10.1084/jem.20041196.PubMed CentralView ArticlePubMedGoogle Scholar
- Li Q, Duan L, Estes JD, Ma ZM, Rourke T, Wang Y, Reilly C, Carlis J, Miller CJ, Haase AT : Peak SIV replication in resting memory CD4+ T cells depletes gut lamina propria CD4+ T cells. Nature. 2005, 434: 1148-1152.PubMedGoogle Scholar
- Mattapallil JJ, Douek DC, Hill B, Nishimura Y, Martin M, Roederer M: Massive infection and loss of memory CD4+ T cells in multiple tissues during acute SIV infection. Nature. 2005, 434: 1093-1099. 10.1038/nature03501.View ArticlePubMedGoogle Scholar
- Reeves RK, Gillis J, Wong FE, Johnson RP: Vaccination with SIVmac239Deltanef activates CD4+ T cells in the absence of CD4 T-cell loss. J Med Primatol. 2009, 38 (Suppl 1): 8-16. 10.1111/j.1600-0684.2009.00370.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Picker LJ, Reed-Inderbitzin EF, Hagen SI, Edgar JB, Hansen SG, Legasse A, Planer S, Piatak M, Lifson JD, Maino VC, Axthelm MK, Villinger F: IL-15 induces CD4 effector memory T cell production and tissue emigration in nonhuman primates. J Clin Invest. 2006, 116: 1514-1524. 10.1172/JCI27564.PubMed CentralView ArticlePubMedGoogle Scholar
- Okoye A, Park H, Rohankhedkar M, Coyne-Johnson L, Lum R, Walker JM, Planer SL, Legasse AW, Sylwester AW, Piatak M, Lifson JD, Sodora DL, Villinger F, Axthelm MK, Schmitz JE, Picker LJ: Profound CD4+/CCR5+ T cell expansion is induced by CD8+ lymphocyte depletion but does not account for accelerated SIV pathogenesis. J Exp Med. 2009, 206: 1575-1588. 10.1084/jem.20090356.PubMed CentralView ArticlePubMedGoogle Scholar
- Rud EW, Cranage M, Yon J, Quirk J, Ogilvie L, Cook N, Webster S, Dennis M, Clarke BE: Molecular and biological characterization of simian immunodeficiency virus macaque strain 32 H proviral clones containing nef size variants. J Gen Virol. 1994, 75 (Pt 3): 529-543. 10.1099/0022-1317-75-3-529.View ArticlePubMedGoogle Scholar
- Stebbings R, Stott J, Almond N, Hull R, Lines J, Silvera P, Sangster R, Corcoran T, Rose J, Cobbold S, Gotch F, McMichael A, Walker B: Mechanisms of protection induced by attenuated simian immunodeficiency virus. II. Lymphocyte depletion does not abrogate protection. AIDS Res Hum Retroviruses. 1998, 14: 1187-1198. 10.1089/aid.1998.14.1187.View ArticlePubMedGoogle Scholar
- Qin S, Rottman JB, Myers P, Kassam N, Weinblatt M, Loetscher M, Koch AE, Moser B, Mackay CR: The chemokine receptors CXCR3 and CCR5 mark subsets of T cells associated with certain inflammatory reactions. J Clin Invest. 1998, 101: 746-754. 10.1172/JCI1422.PubMed CentralView ArticlePubMedGoogle Scholar
- Balashov KE, Rottman JB, Weiner HL, Hancock WW: CCR5 (+) and CXCR3 (+) T cells are increased in multiple sclerosis and their ligands MIP-1alpha and IP-10 are expressed in demyelinating brain lesions. Proc Natl Acad Sci USA. 1999, 96: 6873-6878. 10.1073/pnas.96.12.6873.PubMed CentralView ArticlePubMedGoogle Scholar
- Ebert LM, McColl SR: Up-regulation of CCR5 and CCR6 on distinct subpopulations of antigen-activated CD4+ T lymphocytes. J Immunol. 2002, 168: 65-72.View ArticlePubMedGoogle Scholar
- Loetscher P, Uguccioni M, Bordoli L, Baggiolini M, Moser B, Chizzolini C, Dayer JM: CCR5 is characteristic of Th1 lymphocytes. Nature. 1998, 391: 344-345. 10.1038/34814.View ArticlePubMedGoogle Scholar
- Olsson J, Poles M, Spetz AL, Elliott J, Hultin L, Giorgi J, Andersson J, Anton P: Human immunodeficiency virus type 1 infection is associated with significant mucosal inflammation characterized by increased expression of CCR5, CXCR4, and beta-chemokines. J Infect Dis. 2000, 182: 1625-1635. 10.1086/317625.View ArticlePubMedGoogle Scholar
- Oki M, Ohtani H, Kinouchi Y, Sato E, Nakamura S, Matsumoto T, Nagura H, Yoshie O, Shimosegawa T: Accumulation of CCR5+ T cells around RANTES+ granulomas in Crohn's disease: a pivotal site of Th1-shifted immune response?. Lab Invest. 2005, 85: 137-145.View ArticlePubMedGoogle Scholar
- Sallusto F, Geginat J, Lanzavecchia A: Central memory and effector memory T cell subsets: function, generation, and maintenance. Annu Rev Immunol. 2004, 22: 745-763. 10.1146/annurev.immunol.22.012703.104702.View ArticlePubMedGoogle Scholar
- Clarke S, Almond N, Berry N: Simian immunodeficiency virus Nef gene regulates the production of 2-LTR circles in vivo. Virology. 2003, 306: 100-108. 10.1016/S0042-6822(02)00043-0.View ArticlePubMedGoogle Scholar
- Ling B, Veazey RS, Hart M, Lackner AA, Kuroda M, Pahar B, Marx PA: Early restoration of mucosal CD4 memory CCR5 T cells in the gut of SIV-infected rhesus predicts long term non-progression. AIDS. 2007, 21: 2377-2385. 10.1097/QAD.0b013e3282f08b32.View ArticlePubMedGoogle Scholar
- Monceaux V, Viollet L, Petit F, Cumont MC, Kaufmann GR, Aubertin AM, Hurtrel B, Silvestri G, Estaquier J: CD4+ CCR5+ T-cell dynamics during simian immunodeficiency virus infection of Chinese rhesus macaques. J Virol. 2007, 81: 13865-13875. 10.1128/JVI.00452-07.PubMed CentralView ArticlePubMedGoogle Scholar
- Jin X, Bauer DE, Tuttleton SE, Lewin S, Gettie A, Blanchard J, Irwin CE, Safrit JT, Mittler J, Weinberger L, Kostrikis LG, Zhang L, Perelson AS, Ho DD: Dramatic rise in plasma viremia after CD8(+) T cell depletion in simian immunodeficiency virus-infected macaques. J Exp Med. 1999, 189: 991-998. 10.1084/jem.189.6.991.PubMed CentralView ArticlePubMedGoogle Scholar
- Schmitz JE, Kuroda MJ, Santra S, Sasseville VG, Simon MA, Lifton MA, Racz P, Tenner-Racz K, Dalesandro M, Scallon BJ, Ghrayeb J, Forman MA, Montefiori DC, Rieber EP, Letvin NL, Reimann KA: Control of viremia in simian immunodeficiency virus infection by CD8+ lymphocytes. Science. 1999, 283: 857-860. 10.1126/science.283.5403.857.View ArticlePubMedGoogle Scholar
- Metzner KJ, Jin X, Lee FV, Gettie A, Bauer DE, Di Mascio M, Perelson AS, Marx PA, Ho DD, Kostrikis LG, Connor RI: Effects of in vivo CD8(+) T cell depletion on virus replication in rhesus macaques immunized with a live, attenuated simian immunodeficiency virus vaccine. J Exp Med. 2000, 191: 1921-1931. 10.1084/jem.191.11.1921.PubMed CentralView ArticlePubMedGoogle Scholar
- Lifson JD, Rossio JL, Piatak M, Parks T, Li L, Kiser R, Coalter V, Fisher B, Flynn BM, Czajak S, Hirsch VM, Reimann KA, Schmitz JE, Ghrayeb J, Bischofberger N, Nowak MA, Desrosiers RC, Wodarz D: Role of CD8(+) lymphocytes in control of simian immunodeficiency virus infection and resistance to rechallenge after transient early antiretroviral treatment. J Virol. 2001, 75: 10187-10199. 10.1128/JVI.75.21.10187-10199.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Sallusto F, Lenig D, Förster R, Lipp M, Lanzavecchia A: Two subsets of memory T lymphocytes with distinct homing potentials and effector functions. Nature. 1999, 401: 708-712. 10.1038/44385.View ArticlePubMedGoogle Scholar
- Amyes E, McMichael AJ, Callan MF: Human CD4+ T cells are predominantly distributed among six phenotypically and functionally distinct subsets. J Immunol. 2005, 175: 5765-5773.View ArticlePubMedGoogle Scholar
- Nethe M, Berkhout B and van der Kuyl AC: Retroviral superinfection resistance. Retrovirology. 2005, 2: 52-64. 10.1186/1742-4690-2-52.PubMed CentralView ArticlePubMedGoogle Scholar
- Pandrea I, Apetrei C, Gordon S, Barbercheck J, Dufour J, Bohm R, Sumpter B, Roques P, Marx PA, Hirsch VM, Kaur A, Lackner AA, Veazey RS, Silvestri G: Paucity of CD4+CCR5+ T cells is a typical feature of natural SIV hosts. Blood. 2007, 109: 1069-1076. 10.1182/blood-2006-05-024364.PubMed CentralView ArticlePubMedGoogle Scholar
- Picker LJ, Hagen SI, Lum R, Reed-Inderbitzin EF, Daly LM, Sylwester AW, Walker JM, Siess DC, Piatak M, Wang JC, Allison DB, Maino VC, Lifson JD, Kodama T, Axthelm MK: Insufficient production and tissue delivery of CD4+ memory T cells in rapidly progressive simian immunodeficiency virus infection. J Exp Med. 2004, 200: 1299-1314. 10.1084/jem.20041049.PubMed CentralView ArticlePubMedGoogle Scholar
- Ferguson D, Wade-Evans A, Elsley W, Sangster R, Silvera P, MacManus S, Davis G, Corcoran T, Berry N, Brown S, Jenkins A, Cowie J, Sethi M, Hull R, Stebbings R, Lines J, Norley S, Stott EJ, Almond N: Preparation and characterization of new challenge stocks of SIVmac32 H J5 following rapid serial passage of virus in vivo. J Med Primatol. 2007, 36: 131-142. 10.1111/j.1600-0684.2007.00224.x.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.