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CD4+CD25+ T regulatory cells from FIV+ cats induce a unique anergic profile in CD8+lymphocyte targets
Retrovirologyvolume 7, Article number: 97 (2010)
Using the FIV model, we reported previously that CD4+CD25+ T regulatory (Treg) cells from FIV+ cats are constitutively activated and suppress CD4+CD25- and CD8+ T cell immune responses. In an effort to further explore Treg-mediated suppression, we asked whether Treg cells induce anergy through the alteration of production of cyclins, cyclin-dependent kinases and their inhibitors.
Lymphocytes were obtained from control or FIV+ cats and sorted by FACS into CD4+CD25+ and CD8+ populations. Following co-culture with CD4+CD25+ cells, CD8+ targets were examined by Western blot for changes in cyclins D3, E and A, retinoblastoma (Rb) protein, as well as the cyclin dependent kinase inhibitor p21cip1. Following co-culture with CD4+CD25+cells, we observed up-regulation of p21cip1 and cyclin E, with down-regulation of cyclin D3, in CD8+ cells from FIV+ cats. As expected, CD8+ targets from control cats were quiescent with little up-regulation of p21cip1 and cyclin E. There was also a lack of Rb phosphorylation in CD8+ targets consistent with late G1 cell cycle arrest. Further, IL-2 mRNA was down regulated in CD8+ cells after co-culture with CD4+CD25+ Treg cells. Following CD4+CD25+ co-culture, CD8+ targets from FIV+ cats also had increased Foxp3 mRNA expression; however, these CD8+Foxp3+ cells did not exhibit suppressor function.
Collectively, these data suggest that CD4+CD25+ Treg cells from FIV+ cats induce CD8+ anergy by disruption of normal G1 to S cell cycle progression.
Using FIV as an AIDS lentivirus model, we reported previously that CD4+CD25+ Treg cells in both the acute phase and long-term, asymptomatic phase of infection are constitutively activated and suppress CD4+CD25- and CD8+ T cell immune responses [1–3]. Activated feline Treg cells from FIV+ cats suppress CD4+ cell proliferation and IL-2 production and CD8+ cell IFNγ production [1, 3, 4]. We have demonstrated preferential in vitro and in vivo replication of FIV in the CD4+CD25+ subset, suggesting a unique relationship between lentiviral infections and Treg cell activation [4, 5]. Impaired CD8+ T cell immune responses are well described in AIDS lentivirus infections and evidence suggests that this impairment correlates with activation of CD4+CD25+ Treg cells [6–9].
Lentivirus infections are characterized by an early increase in CD8+ T lymphocyte numbers, and the quality of the CTL response is associated with a decline in plasma viremia. A strong CTL response correlates with clearance of virus from circulation, and a weaker response is associated with poor or no control of viral replication [10–15]. Experimental models and clinical data from other types of viral infections have clearly demonstrated that CD8+ lymphocytes are critical for the control of viral infection, and escape of this initial response can lead to establishment and maintenance of a persistent infection and may contribute to immune exhaustion [16–22]. Using the FIV model we designed experiments to identify lentiviral mechanism(s) used to escape virus elimination and establish a chronic infection in the face of a robust CD8+ response. These experiments have focused on Treg cell activation kinetics during FIV infection, the mechanism of Treg mediated suppression, and identification of cells targeted for Treg-mediated suppression; and we have clearly established that Treg cells are able to suppress CD8+ effector responses during both acute and chronic FIV infection [1–3]. We therefore asked what intracellular events occur in the CD8+ target cell following interaction with CD4+CD25+ Treg cells, do these intracellular events contribute to CD8+ anergy, and could these CD8+ targets be converted into CD8+ suppressor cells?
Down-regulation of IL-2 production, loss of effector function, and lack of proliferation are well described in lymphocyte target cells following interaction with activated CD4+CD25+ Treg cells [1, 23–25]. However, these events are the end result of a complex process, including interruption of cell cycling events, that may occur in CD4+CD25- or CD8+ target cells following their interaction with CD4+CD25+ Treg cells. Cell cycle progression is tightly regulated by proteins such as cyclins, cyclin dependent kinases (CDKs) and cyclin dependent kinase inhibitors (CDKIs) that ensure an appropriate and coordinated cellular response. This mechanism responds to intracellular and extracellular signals and will arrest cell cycle progression (induce anergy) in response to adverse intracellular or extracellular conditions . During the early immune response, primary T lymphocytes that receive optimal stimulation through their TCR and co-stimulatory pathways proceed through G1 cell cycle progression (Figure 1). Subsequent multiple cell divisions are then required during this primary response for optimal IL-2 and IFNγ production and the avoidance of anergy [27, 28]. Responding to stimulation under favorable conditions, D cyclins are expressed sequentially starting in late G0/early G1 during the normal progression of the cell cycle [28, 29]. Next, Cyclin E emerges during late G1 phase following degradation/sequestration of the CDKIs p27Kip1 and p21Cip1. The CDKIs p27Kip1 and p21Cip1 are instrumental in a coordinated G1 to S phase transition "holding" the cellular machinery in place until the cyclins and CDKs are at the proper levels and activation state. Cyclins partner with their cyclin dependent kinase to sequentially phosphorylate Rb during G1 progression. Hyperphosphorylation of Rb and release of E2F transcription factors signals the irreversible commitment to S phase and cell cycle progression [28, 29].
There are at least two broad categories of CD4+CD25+ Treg cells, natural Treg cells and adaptive (or induced) Tregs [30, 31]. Natural Treg cells originate in the thymus and reside in peripheral lymph tissues to prevent autoimmune responses [32, 33]. Adaptive Treg cells are phenotypically indistinguishable from natural Treg cells and modulate immune responses to microbial pathogens including bacteria, viruses, fungi, and intracellular parasites [34–36]. A third population of regulatory cells, Foxp3+CD8+ regulatory lymphocytes has also been described [37–40]. The derivation of Foxp3+CD8+ regulatory lymphocytes is not completely understood, however like their CD4+Foxp3+ counterparts, it is plausible that there is both a "natural" and "adaptive" subset of these cells. Foxp3 is a forkhead transcription factor which binds DNA adjacent to NFAT sites and is essential to the development of CD4+CD25+ regulatory T cells [41–43]. We and others have shown that Foxp3 expression can be induced in CD4+CD25- target cells under certain conditions and that these induced Foxp3+ cells exhibit suppressor activity [44, 45]. Stable Foxp3 expression is essential for Treg development and function, but is not exclusive to regulatory T cells, as transient or unstable Foxp3 expression has been observed in other T cell subsets, suggesting that Foxp3 may play other roles in T cell homeostasis [46–48].
Because activated Treg cells are known to induce anergy in T cell targets and because FIV infection activates Treg cells, we asked whether activated Treg cells from FIV+ cats altered the expression of cyclins, cyclin-dependent kinases and cyclin-dependent kinase inhibitors that regulate anergy in CD8+ target cells. In FIV infection, CD8+ lymphocytes display an activated phenotype, yet have compromised effector function, reminiscent of anergy [3, 13, 14]. It is likely that CD8+ lymphocytes receive both stimulatory and inhibitory signals, leading to a complex convergence of intracellular signaling events. We therefore systematically evaluated cell cycle proteins, starting with G1 phase proteins, in an effort to determine when and if anergy occurs in CD8+ lymphocyte targets following their interaction with activated Treg cells. To further define the relationship between activated Treg cells and CD8+ targets in FIV infected cats, we asked if Treg cells from chronically infected FIV+ cats might also induce suppressor function in CD8+ target cells following co-culture.
Cyclin D3 production is decreased and cyclin E production is increased in CD8+ targets from FIV+ cats following CD4+CD25+co-culture
To examine the effect of FIV infection on cell cycle regulatory proteins that could explain T cell-mediated anergy, cyclin D3 was examined first during sequential evaluation of cell cycle proteins in CD8+ target cells. In T lymphocytes, cyclin D3 typically assembles with CDK4 or CDK6 during mid G1 phase and reaches maximal production during late G1/early S phase (Figure 1[28, 29]). Lymph node CD8+ cells from either FIV+ or FIV- cats were untreated or co-cultured with CD4+CD25+ Treg cells. In both FIV+ and FIV- cats, cyclin D3 was modestly reduced in CD8+ cells following a twelve hour co-culture with CD4+CD25+ Treg cells (Figure 2, Additional file 1, Table S1).
Because cyclin E emerges in late G1 to facilitate G1 to S transition, we asked whether there was any change in cyclin E in CD8+ targets following CD4+CD25+ co-culture. As shown in Figure 3 and supplemental table 1, there was a greater than 2 fold increase in cyclin E production in CD8+ targets from FIV+ cats with a moderate decrease in cyclin E production in FIV- control cats.
The CDKI p21Cip1 is increased in CD8+ target cells from chronically infected FIV+ cats following CD4+CD25+co-culture
We asked if activated Treg cells from FIV-infected cats might induce CDKI production in lymphocyte targets, because increased CDKI production correlates with cell cycle arrest in lymphocytes [28, 29, 49, 50]. The Ink 4 family of CDKIs, such as p15Ink4b, can antagonize the assembly of cyclin D-dependent kinases . The Cip/Kip family of CDKIs includes p21Cip1 and p27Kip1 which bind cyclins D, E, and A . The CDKI p21Cip1 helps control the activation and survival of autoreactive T cells and overproduction is associated with G1 cell cycle arrest [28, 50, 51]. There was greater than a 1.5 fold increase in p21Cip1 in CD8+ targets from FIV+ cats following a twelve-hour CD4+CD25+ co-culture, while only a slight reduction in p21Cip1 was observed in CD8+ targets from FIV- cats following a twelve-hour CD4+CD25+ co-culture (Figure 4, Additional file 1, Table S1). The levels of both p15Ink4b and p27Kip1 production in CD8+ targets following CD4+CD25+ co-culture were unchanged (Additional file 2, Figure S1).
Hyperphosphorylation of Rb is not evident in CD8+ target cells following CD4+CD25+co-culture
Collectively, the results of Figures 2, 3 and 4 demonstrate that cyclin D3 levels have declined while cyclin E and p21Cip1 levels have increased. This profile could be consistent with one of two outcomes: either the target cell has progressed to S phase or the cell has undergone late G1 cell cycle arrest. In an effort to clearly delineate late G1 cell cycle arrest from early S phase transition, we examined Rb phosphorylation status. Hyperphosphorylation of Rb allows release of the E2F family of transcription factors and signals irreversible S phase commitment [27, 29]. Rb protein hyperphosphorylation was not evident in CD8+ target cells following an eighteen hour CD4+CD25+ co-culture (Figure 5, Additional file 1, Table S1). In sum, the findings of Figures 2, 3, 4 and 5 are most consistent with CD4+CD25+ Treg-induced anergy in CD8+ target cells from FIV+ cats (Figure 6).
IL-2 mRNA expression is reduced in CD8+ target cells from chronically infected FIV+ cats following CD4+CD25+co-culture
Lymphocyte activation is regulated by cyclin-dependent kinases that stimulate the production of IL-2 mRNA [27, 28, 50, 52, 53]. Autocrine and paracrine production of IL-2 is critical to lymphocyte expansion, differentiation, and the avoidance of anergy [54–57]. Therefore, we examined IL-2 mRNA to validate the findings in Figures 2, 3, 4, 5 and 6. There was a greater than four-fold reduction in IL-2 mRNA in stimulated CD8+ lymphocytes from FIV+ cats following CD4+CD25+ co-culture as compared to stimulated CD8+ lymphocytes alone, consistent with the induction of anergy (Figure 7).
Foxp3 expression is increased in CD8+ targets from FIV+ cats following CD4+CD25+ co-culture, but CD8+target cells lack suppressor function
We asked whether the CD8+ target cells from FIV+ cats shown in Figures 2, 3, 4, 5, 6 and 7 might upregulate Foxp3 and exhibit suppression of autologous CD8+ responses. As shown in Figure 8a, Foxp3 induction in FIV+ cats was maximal in ConA stimulated (5 ug/ml), CD8+ lymphocytes following a 24 hour CD4+CD25+ co-culture (p < 0.05). Foxp3 levels did not increase any further following a 48 hour co-culture (data not shown). To assess suppressive potential following co-culture, CD8+ target cells and CD4+CD25+ Treg cells were then re-sorted and combined with autologous CD8+ lymphocytes to assay IFNγ production. Figure 8b demonstrates that CD4+CD25+ cells from FIV+ cats inhibited CD8+ IFNγ spot forming cells (SFCs) by approximately twenty-five percent. However, in the same experiment, CD8+ lymphocytes previously co-cultured with the same CD4+CD25+ cells lacked suppressor function despite upregulation of Foxp3.
The mechanisms underlying T cell immune dysfunction during the course of AIDS lentiviral infections are still not completely understood. One of the more puzzling aspects of these infections is the presence of lymphocytes that appear to be activated yet exhibit compromised effector function [14, 58]. This laboratory and others have documented Treg mediated immune suppression of both CD4+CD25- and CD8+ lymphocytes during acute and chronic AIDS lentiviral infection [1–3, 7, 8]. Based upon these data, the authors have explored the intracellular events in the CD8+ target cells, following co-culture with CD4+CD25+ Treg cells, for a clearer understanding of what may contribute to CD8+ immune dysfunction. As CD8+ lymphocytes are important for both the elimination of acute viral infections and control of chronic viral infections, understanding Treg-mediated CD8+ anergy may be one of the keys to understanding AIDS associated immune dysfunction.
As T cell anergy appears to be an important component to virus induced immune dysfunction, we studied production of molecules that regulate both cell cycle progression and cellular anergy. Because the control of cell cycle progression versus cell cycle anergy is regulated by the relative production of selected cell cycle proteins during the G1 to S phase transition; we examined a number of these proteins in CD8+ T cells anergized by contact with activated CD4+CD25+ Treg cells from FIV infected cats. As shown in Figure 2, there was a modest decrease in cyclin D3 following a twelve hour Treg co-culture. In general, cyclin D3 levels are expected to increase during the progression from G1 to S phase, suggesting that the CD8+ target cells had either progressed well into S phase, or had begun G1 cell cycle arrest . Cyclin E emerges during the progression from G1 to S phase and Figure 3 clearly shows an increase in cyclin E in FIV+ cats following a twelve hour Treg co-culture, while there was a moderate decrease in cyclin E in FIV- cats. Cyclin A emerges during early S phase and progressively increases during S phase . There was no change in cyclin A activity evident following an eighteen hour Treg co-culture. The lack of increased cyclin A activity suggests that the cells were in very late G1 cell cycle arrest (Additional file 2, Figure S1). Next, the CDKI p21cip1 was examined. This CDKI is reported to have a complex role in cell cycle regulation by facilitating the activity of the D cyclin family, while inhibiting the activity of cyclin E [28, 49]. As shown in Figure 4 and Figure 6, in CD8+ target cells from FIV+ cats, p21cip1 was increased by approximately 1.7 fold, following co-culture with CD4+CD25+ Treg cells. During the course of G1 progression, Rb is sequentially phosphorylated at different sites by cyclin/CDK complexes, which facilitates the release of E2F transcription factors, marking the irreversible commitment to S phase . Therefore, increases in intracellular cyclin E, should be followed by Rb hyperphosphorylation if the cell progresses into S phase. As shown in Figure 5, there was no Rb hyper-phosphorylation evident following Treg co-culture, suggesting that both cyclin D and cyclin E failed to phosphorylate Rb.
In fibroblasts and CD4+ lymphocytes during normal cell cycle progression, p21cip1 reaches maximal production levels during S phase [28, 59]. However, in different models of liver disease, increased p21cip1 production is associated with G1 cell cycle arrest . Conversely, p21cip1 knockout mice exhibit shorter G1 to S phase transition times and greater proliferative capacity . A recent report by Bergamashi et al  has demonstrated increased p21cip1 production in macrophages from HIV-infected individuals that may be associated with inhibition of viral replication within the macrophage. These findings suggest that increased p21cip1 production in CD8+ targets is likely associated with late G1 cell cycle arrest. The upregulation of p21cip1 may provide a beneficial effect to the host by creating a poor environment for viral replication while conversely contributing to the development of immunodeficiency by halting CD8+ effector and proliferative responses.
The findings in Figures 2, 3, 4, 5 and 6 are consistent with late G1 cell cycle arrest and anergy. To further characterize this interaction, we asked if Treg cells from FIV+ cats would suppress IL-2 mRNA expression in autologous CD8+ targets. The ability to produce IL-2 is a reflection of lymphocyte activation, because it requires a convergence of intracellular events, including cyclin-dependent kinase activation of E2F transcription factors [27, 28, 50, 52, 53]. Initially, exogenous signals are critical to stimulating the CD8+ cell to produce IL-2 for lymphocyte expansion, differentiation, and the avoidance of anergy [54–57]. As shown in Figure 7, CD8+ lymphocytes were stimulated with ConA to promote IL-2 production. Lymphocytes from FIV- cats exhibited very modest increases in IL-2 mRNA following ConA stimulation, likely because these cats were SPF animals with little antigenic exposure and a relatively quiescent immune system. This is similar to our previous observation that CD8+ lymphocytes from FIV-, SPF cats produce very little IFNγ mRNA following ConA stimulation . The CD8+ lymphocytes from FIV+ cats exhibited a marked increase in IL-2 mRNA following ConA stimulation which was then markedly decreased following co-culture with CD4+CD25+ Treg cells. Taken together, the findings of decreased cyclin D3 production, increased cyclin E and p21cip1 production, lack of cyclin A production, lack of Rb phosphorylation, combined with suppression of IL-2 mRNA in CD8+ targets suggests that Treg cells from FIV+ cats are able to induce very late G1 cell cycle arrest in CD8+ targets. This also may help to explain, in part, why CD8+ lymphocytes from FIV+ cats display an activated phenotype yet have marginal effector function.
There is a degree of plasticity in T helper versus Treg phenotype and function; for example, under appropriate stimulating conditions, CD4+ T cells exhibiting T helper phenotype and function can be converted into Treg (or Treg "like") cells [44, 45]. As demonstrated in murine models and in FIV infection, these converted cells express Foxp3 and suppress T helper effector responses [44, 45]. There is also evidence for expansion of CD8+Foxp3+ suppressor cells in the SIV lentivirus model . Therefore, we asked if Foxp3 might also be up-regulated in CD8+ targets from FIV+ cats following Treg co-culture. We observed CD8+ target cell up-regulation of Foxp3 following CD4+CD25+ co-culture, however, these target cells lacked suppressor function (Figure 8). Our results are consistent with those also reported by Dieckmann et al.  who demonstrated that activated Treg cells co-cultured with CD8+ target cells suppressed effector function and induced anergy in CD8+ targets, but did not convert these cells into CD8+ suppressor cells. Recent reports demonstrate that Foxp3 expression can be transiently induced in human CD4+ and CD8+ T lymphocyte targets without these cells exhibiting regulatory function; however, the function of Foxp3 in these target cells in unclear [46–48]. Further investigation is needed to clarify the role of Foxp3 expression in these cells.
Analysis of proteins involved in cell cycle regulation is consistent with late G1 cell cycle arrest in CD8+ targets from FIV+ cats following CD4+CD25+/CD8+ co-culture (Figures 2, 3, 4, 5 and 6). Figure 7 clearly shows Treg-mediated suppression of IL-2 mRNA production in CD8+ targets and we have recently reported reduced IFNγ production in CD8+ target cells from FIV+ cats following CD4+CD25+ Treg co-culture . Collectively, these data suggest Treg-mediated inhibition of both effector and proliferative functions in CD8+ targets from FIV+ cats. Previous work suggests that CD4+CD25+ Treg cells are activated early and progressively during the course of FIV infection and that inhibition of CD4+CD25- and CD8+ effector responses occurs early and progressively during the course of FIV infection [1–3]. Further understanding of how Treg cells inhibit CD8+ antiviral function and CD4+ T helper function during the course of FIV infection will help to clarify how lentiviruses establish and maintain a persistent infection and may offer insight into the development of novel vaccination and treatment strategies.
Specific pathogen free (SPF) cats were obtained from Liberty Research, Inc. (Waverly, NY) and housed in the Laboratory Animal Resource Facility at the College of Veterinary Medicine, North Carolina State University. FIV infected cats were housed separately from uninfected control cats. Protocols were approved by the North Carolina State University Institutional Animal Care and Use Committee.
Infection with FIV
The NCSU1 isolate of FIV was originally obtained from a naturally infected cat at the North Carolina State University College of Veterinary Medicine and has been described in detail elsewhere . Virus inoculum was grown as a single tissue culture passage in an IL2-dependent feline CD4+ cell line (FCD4-Ecells) as previously described . The cats were infected intravenously with 1 × 105 TCID50 of cell-free virus culture and FIV infection was confirmed on serum samples by using a commercially available ELISA Kit (IDEXX Laboratories). The cats had been infected for approximately 2 years prior to these experiments. Plasma viremia was not assessed at the time of lymphocyte collection for the experiments outlined in Figures 2, 3, 4, 5, 6, 7 and 8. The FIV+ cats in this study had normal lymphocyte counts (mean = 2812/μl) with an inverted CD4:CD8 ratio (mean = 0.61). Control cats were age matched uninfected SPF cats.
Lymphocytes were harvested either by LN excision or following euthanasia. Lymph node biopsies were performed as previously described [2, 65]. Following collection, lymph nodes were processed into a single cell suspension for purification of lymphocyte subsets.
Murine monoclonal anti-feline CD4 (mAb 30A), CD8 (mAb 3.357) and CD25 (mAb 9F23) were produced in our laboratory . The anti-feline CD25 (mAb 9F23) was originally provided by K. Ohno (University of Tokyo). The antibodies were conjugated to FITC (anti-CD8, anti-CD25), PE (anti-CD4, anti-CD8) or biotin (anti-CD8) (developed with Streptavidin/PerCP).
Lymphocyte sorting and culture
Lymphocytes were sorted into CD8+ and CD4+CD25+ populations by FACS, using a Moflo high speed cell sorter. Populations were ~99% pure. Lymphocyte cultures were maintained in serum restricted media (1.0% FBS) in 12 well, flat bottom plates. Following CD8+/CD4+CD25+ co-cultures, CD8+ and CD4+CD25+ cells were then re-sorted by FACS and examined by western blot, PCR or ELISpot.
Reverse transcription real time PCR
2 × 106 CD8+ lymphocytes from FIV- and FIV+ cats were untreated, ConA stimulated (5 ug/ml) for two hours and washed, or ConA stimulated for two hours and washed followed by co-culture with CD4+CD25+ cells for 24 hrs (CD4+CD25+ to CD8+ ratio = 1:1). Following CD8+/CD4+CD25+ co-cultures, CD8+ and CD4+CD25+ cells were then re-sorted by FACS. RNA from cell cultures was isolated using the Qiagen RNeasy plus Mini Kit and reverse transcription was performed using the Promega Reverse Transcription System, following the manufacturer's instructions for both. This reaction was followed by a real-time PCR step using the universal Taqman PCR Mastermix (Applied Biosystems) and the Qiagen Quantitect Sybr Green PCR Kit (probe). The reactions were run in duplicates in 96 well plates. The fold induction was calculated by using the ΔΔCt value, where Fold Induction = 2 - (ΔΔCt), as described by Winer et al . PBMCs from an FIV negative cat and GAPDH as the internal control were used as the calibration sample value in the ΔΔCt equation. The feline specific IL-2, Foxp3, and GAPDH primer sequences utilized for the real time PCR reaction were as follows: IL-2 (forward ACA GTG CAC CTG CTT CAA GCT CT-3' and reverse CCT GGA GAG TTT GGG GTT CTC AGG), Foxp3 (forward GCC TGC CAC CTG GAA TCA AC and reverse GTG TGC TGG GGC TTG GGA), and GAPDH (forward GGA GAA GGC TGG GGC TCA C and reverse GGT GCA GGA GGC ATT GCT GA).
Approximately 4 × 106 CD8+ FACS purified CD8+ and CD4+CD25+ lymphocytes were harvested for each treatment group. For co-culture experiments, CD8+ and CD4+CD25+ were co-cultured at a 1:1 ratio and then re-sorted using FACS (~99% purity). The CD8+ cells were then lysed with NP-40 and separated by SDS-Page. The blots were analyzed using anti-cyclin D3 (Cell Signaling Technologies #2936), anti-Cyclin E (Cell Signaling Technologies #4129), anti-p21 (Novus Biologicals #NB-120-14061), and anti-Rb (Cell Signaling Technologies #9308), followed by HRP-conjugated goat anti-mouse IgG1 and detected by chemiluminescence. The blots were then stripped and re-probed with anti-actin and HRP-conjugated goat anti-mouse. For each treatment group, actin and the protein in question were evaluated by photodensitometry and normalized using the VersaDoc imaging system (Bio-Rad Laboratories). For reporting of fold change, each treatment group was compared to unstimulated CD8+ controls which were assigned a value of 1.
Following co-culture, CD4+CD25+ cells and CD8+ target cells were re-sorted, assessed by trypan blue staining for viability (<10% positive), and then cultured alone (2.5 × 105 per well) or co-cultured with ConA stimulated autologous CD8+ lymphocytes (1:1 ratio) for 48 hrs in pre-coated 96 well ELISpot plates (monoclonal anti-feline IFNγ, R and D systems). The ConA stimulated CD8+ lymphocyte targets were stimulated for two hours then washed prior to co-culture. The plates were incubated for 24 hours, stained with detection antibody, and developed per the manufacturer's instructions. Once dry, each well was counted with an automated ELISpot reader for quantification of spot forming cells (SFC) per number of cells plated in each well. Percent suppression was calculated by the following: (1) ConA stimulated CD8+ lymphocyte SFCs ÷ ConA stimulated CD8+ lymphocytes + Foxp3+ CD8+ lymphocytes SFCs or (2) ConA stimulated CD8+ lymphocyte SFCs ÷ ConA stimulated CD8+ lymphocytes + CD4+CD25+ lymphocytes SFCs. CD4+CD25+ lymphocytes alone and CD8+Foxp3+ alone did not produce any IFNγ SFCs.
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This work was funded in part by National Institute of Health grants AI080288 (MBT) and 1K08AI074445 (JEF). The authors would like to recognize Lawana Hartsell, Janet Dow, and Deb Anderson for their excellent technical assistance.
The authors declare that they have no competing interests.
JF carried out all of the studies contained in this manuscript and drafted the manuscript. WT assisted with study design, data interpretation and manuscript revisions. MT assisted with study design, data interpretation and manuscript revisions. All authors read and approved the final manuscript.