- Open Access
Dendritic cell-mediated HIV-1 transmission to T cells of LAD-1 patients is impaired due to the defect in LFA-1
Retrovirologyvolume 3, Article number: 75 (2006)
Dendritic cells (DC) have been proposed to mediate sexual HIV-1 transmission by capturing the virus in the mucosa and subsequently presenting it to CD4+ T cells. We have demonstrated before that DC subsets expressing higher levels of intercellular adhesion molecule-1 (ICAM-1) are better HIV-1 transmitters. ICAM-1 binds leukocyte function-associated molecule-1 (LFA-1) on T cells, an integrin responsible for adhesion and signaling at the immunological synapse. To corroborate the importance of the ICAM-1— LFA-1 interaction, we performed transmission experiments to LFA-1 negative leukocytes from Leukocyte Adhesion Deficiency type 1 (LAD-1) patients.
We clearly show that DC-mediated HIV-1 transmission to LAD-1 T cells is impaired in comparison to healthy controls. Furthermore, HIV-1 transmission to T cells from a unique LAD-1 patient with a well characterized LFA-1 activation defect was impaired as well, demonstrating that activation of LFA-1 is crucial for efficient transmission. Decreased cell adhesion between DC and LAD-1 T cells could also be illustrated by significantly smaller DC-T cell clusters after HIV-1 transmission.
By making use of LFA-1 defect cells from unique patients, this study provides more insight into the mechanism of HIV-1 transmission by DC. This may offer new treatment options to reduce sexual transmission of HIV-1.
One of the first cell types encountered by HIV-1 during sexual transmission are intraepithelial and submucosal dendritic cells (DC) [1–3]. DC are professional antigen-presenting cells that sample the environment at sites of pathogen entry. Sentinel immature DC (iDC) develop into mature effector DC (mDC) upon activation by microorganisms or inflammatory signals, and migrate to the draining lymph nodes where they encounter and stimulate naïve Th cells [4, 5]. HIV-1 has been proposed to make use of this migratory process, being captured by DC and delivered to the lymph node where the virus is transmitted to CD4+ T cells. In addition to this, DC can facilitate local HIV-1 replication in mucosal T cells [6, 7]. HIV-1 transmission by DC takes place via cell-cell contact through an 'infectious synapse' [8, 9].
We have shown before that intercellular adhesion molecule-1 (ICAM-1) expression on DC is crucial for HIV-1 transmission to T cells: Monocyte-derived DC subsets that express higher levels of ICAM-1 show higher HIV-1 transmission efficiencies to T cells , and transmission by both monocyte-derived DC and DC isolated from blood can be inhibited with blocking antibodies against ICAM-1 [8, 10]. During antigen presentation, ICAM-1 expressed by DC binds to T cells via leukocyte function-associated molecule-1 (LFA-1). This interaction plays a key role in the initiation of immune responses by strengthening the adhesion between DC and T cells at the immunological synapse [11–13]. LFA-1 is an integrin composed of the non-covalently bound α L-subunit CD11a and β2-subunit CD18 . Lack of proper β2 expression due to a deletion or mutation in the CD18 gene leads to Leukocyte Adhesion Deficiency type-1 (LAD-1). Patients with this rare recessive disorder suffer from impaired wound healing without pus formation and recurring necrotic soft tissue infections. As CD11/CD18 heterodimers pair intracellularly, LFA-1 is not expressed at the cell surface of leukocytes from LAD-1 patients. The migration of leukocytes from the bloodstream into inflamed tissue is consequently hampered. In healthy individuals, stimulation of rolling leukocytes along endothelial cell lining induces a conformational change of CD11/CD18 heterodimers from a low to a high ligand-binding state, bringing cells to a halt. As expected, this adhesive process is impaired in LAD-1 patients [15–19]. A unique variant of the LAD-1 disorder has been described (LAD-1/variant syndrome) . Cells of this patient with clinical features of a mild LAD-1 disorder do express LFA-1, but cellular activation does not result in activation of LFA-1, i.e. the 'inside-out signaling' that is necessary for increased ICAM-1 binding is impaired [12, 20–22].
To further corroborate the importance of LFA-1 in HIV-1 transmission, we made use of T cells from LAD-1 patients. We found that DC-mediated HIV-1 transmission to LFA-1 negative T cells is impaired in comparison to healthy controls. Furthermore, HIV-1 transmission to T cells isolated from the unique LAD-1/variant patient is impaired too, meaning that not only recognition of ICAM-1 but also high-activity binding is important for efficient transmission. Finally, we show that one day after HIV-1 transmission, DC-T cell clusters of LAD-1 and LAD-1/variant cells are significantly smaller than control clusters, which is illustrative for the reduced cell-cell adhesion in LAD-1 patients. By making use of cells isolated from unique patients, this study provides more insight into DC-mediated HIV-1 transmission, which may offer new options to inhibit HIV-1 transmission.
DC-mediated transmission to LAD-1 T cells is impaired
To investigate the importance of the ICAM-1— LFA-1 interaction in DC-mediated HIV-1 transmission, we performed transmission experiments with DC obtained from healthy donors and peripheral blood leukocytes (PBL) from LAD-1 patients or healthy controls. We isolated leukocytes from three different LAD-1 patients, whose characteristics are given in Table 1. To confirm the negative LFA-1 status of LAD-1 leukocytes, we performed FACS analysis on CD11a and CD18, of which one representative patient and control are depicted in Fig. 1, upper two panels. We further determined by FACS that the expression of CD4 and CXCR4 was comparable to healthy controls (results not shown). In order to test the transmission efficiency to LAD-1 T cells, we used DC stimulated by poly (I:C) since this subset expresses the highest level of ICAM-1 and is the most efficient HIV-1 transmitter .
We incubated the DC with HIV-1 for 2 hr, followed by washing steps to remove unbound virus. After addition of LAD-1 or control PBL, we determined the transmission efficiency by measuring the accumulation of HIV-1 capsid protein p24 (CA-p24) in T cells by FACS 1–3 days later. To prevent subsequent rounds of HIV-1 replication after transmission in this single-cycle transmission assay, we added an inhibitor of the viral protease (saquinavir, [23, 24]). To distinguish virus transmitted to T cells from HIV in DC, we co-stained with CD3 and DC-SIGN. DC and T cells tend to cluster, which would hamper an accurate estimation of transmission efficiency by FACS. We therefore added EDTA to our FACS buffer to reduce the amount of cell clustering. Indeed, the majority (95%) of the CD3 positive cells was negative for DC-SIGN, showing that only a few DC were attached to T cells during the FACS analysis (Fig. 2A). In uninfected controls of LAD-1 and healthy PBL only background percentages of CA-p24 positive T cells were scored (0.06%, Fig. 2B). Addition of HIV-1 resulted in an increase in CA-p24 positive T cells when using PBL from healthy controls (1.09%, Fig. 2C), whereas only a slight increase was observed in PBL from LAD-1 donors (0.14%, Fig. 2D). The intracellular CA-p24 levels reached a maximum two days after DC-mediated HIV-1 transmission for both control and LAD-1 PBL, which is depicted in Fig. 2E for one representative control and LAD-1 patient. On average, DC-mediated HIV-1 transmission to control T cells was nine times more efficient (Fig. 2F, n = 3).
HIV-1 replication in LFA-1 negative T cells after DC-mediated transmission is delayed
In addition to quantification of the transmission efficiency in a single-cycle transmission assay (Fig. 2), we followed viral replication after transmission (Fig. 3). In this spreading infection assay, we did not add saquinavir to allow cell-cell spread of newly produced virus. The replication of HIV-1 after transmission to LAD-1 PBL is delayed with 1–2 days in comparison to healthy controls (Fig. 2), which reflects the lower transmission efficiency of figure 2. Since CA-p24 levels eventually reach a similar plateau, we conclude that LAD-1 cells are susceptible to HIV-1, but that the transmission is taking place at a lower efficiency.
Activation of LFA-1 is crucial for efficient HIV-1 transmission
In order to efficiently bind ICAM-1, LFA-1 needs to be activated. Cellular activation by chemokines from endothelial cells or by TCR/CD3 cross-linking results in a conformational change of LFA-1 from a low to a high ligand-binding state [12, 21, 25]. We questioned whether LFA-1 expression by T cells is sufficient for efficient HIV-1 transmission by DC, or that additional activation of LFA-1 is necessary. To investigate this, we used cells from a unique patient with mild LAD-1 symptoms (LAD-1/variant). The leukocytes from this patient express LFA-1 (Fig. 1 and Table 1), but the integrin cannot be induced into an active conformation . In comparison to the experiments with LFA-1 negative cells, we obtained similar results: HIV-1 transmission to LAD-1/variant T cells was impaired in the single-cycle assay (Fig. 4A) and replication after transmission was delayed with 2 days (Fig. 4B). This demonstrates that LFA-1 has to be activated to a high ligand-binding state in order to mediate HIV-1 transmission. As an additional control, we infected LAD-1/variant PBL with HIV-1 in the absence of DC (Fig 4C). HIV-1 replication in CD3/CD28 stimulated PBL from the LAD-1/variant patient was comparable to healthy controls, showing that not replication but efficient transmission by DC depends on LFA-1 activation.
LAD-1 and LAD-1/variant T cells form smaller clusters with DC
DC attract T cells and form large clusters in vivo and in vitro, a process that is dependent on cell-cell adhesion [26, 27]. We studied the clusters of DC and leukocytes 24 hr after DC-mediated HIV-1 transmission. The cluster size of DC with T cells from healthy individuals was clearly larger than the clusters with T cells from LAD-1 and LAD-1/variant T cells, as is shown in the photographs (Fig 5A). Quantitative determination of the amount and diameter of clusters showed that although the number of clusters was only slightly reduced (30, 26 and 25 clusters on average for control, LAD-1 and LAD-1/variant respectively), the mean cluster diameter of control cells was significantly larger (9.1 versus 5.6 and 6.2 in arbitrary units for LAD-1 and the variant respectively; p < 0.001 and <0.002). We subsequently grouped the clusters according to diameter (Fig. 5B), and clearly demonstrate that their actual number is not reduced for the LAD-1 and LAD-1/variant T cells, but that they are significantly smaller in size.
In the present study, we demonstrate the role of LFA-1 in HIV-1 transmission by DC. Previously we have shown that ICAM-1 expression on both monocyte-derived DC and DC from blood is critical for HIV-1 transmission [8, 10]. In accordance with this, we now show that DC-mediated transmission to LFA-1-negative T cells from LAD-1 patients is severely impaired. Normally, LFA-1 is activated by different kinds of stimuli, and binding to ICAM-1 is subsequently up-regulated (inside-out signaling) [12, 13, 21, 28]. Currently, it is assumed that activation of LFA-1 may be regulated via changes in affinity (active conformation), avidity (clustering) or both [22, 29–33]. The fact that transmission to T cells of a unique patient (LAD-1/variant syndrome) , with an inside-out signaling deficient LFA-1, was impaired as well, demonstrates for the first time that LFA-1 activation is crucial for DC-mediated HIV-1 transmission. Although LFA-1 of this patient is able to recognize its ligand, no high avidity/affinity binding to ICAM-1 is taking place. Since there is no strong binding to ICAM-1, signaling through LFA-1 into the T cell (outside-in signaling) is probably not taking place either. In healthy individuals, signaling through LFA-1 after ICAM-1 binding leads to actin polymerization and remodeling, which is important for enhanced cell adhesion . Impaired cell adhesion in LAD-1 (and variant) patients can also be illustrated by the significantly smaller clusters of DC with T cells (Fig. 5). A smaller number of T cells that is tightly attached to DC will result in a decrease of the window of opportunity for HIV-1 transmission. Furthermore, it is likely that the creation of an 'infectious synapse' is disturbed in LAD-1 and LAD-1/variant patients. Others have shown that DC-SIGN is an important component of the infectious synapse [9, 35]. Our results strongly indicate that LFA-1 is also important for infectious synapse formation, possibly through cytoskeletal rearrangements that are induced by ICAM-1 binding.
The infectivity and subsequent replication of HIV-1 in T cells can be influenced by T cell activation and proliferation. Due to the young age of the patients and severity of the disease, no more cells could be obtained from these patients to perform a separate mixed lymphocyte reaction (MLR). However, we found no lower cellular proliferation of LAD-1 and LAD-1/variant T cells after co-culture with DC during FACS analysis, nor did we find higher percentages of dead cells. In addition, the leukocytes of the LAD-1/variant patient have been shown to proliferate normally, and have normal calcium influx, actin metabolism and protein kinase activity . Another factor influencing HIV-1 infectivity is the incorporation of host ICAM-1 in budding virions and expression of LFA-1 on target cells [36–40]. To critically test this hypothesis, we performed transmission experiments with HIV-1 produced both in C33A cells and in PM1 T cells. C33A cells do not express ICAM-1 (or LFA-1), yielding virions without ICAM-1. With both virus stocks, we found impaired DC-mediated transmission to T cells of LAD-1/variant and LAD-1 patients, ruling out that the virus-producer cell is of influence. This observation is in concordance with our previous work  and the work of Bounou and co-workers, who showed that in DC-mediated HIV-1 transmission, virion-associated ICAM-1 is of no influence . Furthermore, we have shown that LAD-1/variant and control T cells are equally susceptible to HIV-1 in the absence of DC, demonstrating that the DC-mediated transmission itself is impaired, instead of the ability of HIV-1 to infect these cells.
The importance of the ICAM-1— LFA-1 interaction for DC-T cell contact and HIV-1 transmission suggests a new therapeutic target for the development of transmission-blockers. Interestingly, the fungal metabolite lovastatin, which belongs to the statin compounds used in the treatment of hypercholesterolemia, was shown to bind LFA-1 and inhibit the interaction with ICAM-1 . Furthermore, lovastatin was recently shown to block entry of ICAM-1-containing HIV-1 virion particles into T cells . We therefore tested whether lovastatin could block DC-mediated HIV-1 transmission. Although we measured a significant decrease in HIV-1 transmission, inhibition was due to toxicity of the compound at the micromolar range that is required for blocking the ICAM-1— LFA-1 interaction (results not shown). Given the importance of LFA-1 in HIV-1 transmission by DC, future research should focus on the development of less toxic derivatives or other small molecule inhibitors of the ICAM-1— LFA-1 interaction [44, 45]. Now that there is proof that compounds can be generated that potently inhibit and target integrins like LFA-1  the use of such selective oral compounds may prove very useful in preventing or treating various diseases. With respect to HIV-1 transmission, these compounds can be used in combination with other drugs in a microbicide mixture that will help slowing down the ongoing HIV-1 pandemic.
Materials and methods
Generation of monocyte-derived dendritic cells
Peripheral blood mononuclear cells (PBMC) were isolated from blood of healthy donors by density centrifugation on Lymphoprep (Nycomed, Torshov, Norway). Subsequently, PBMC were layered on a Percoll gradient (Pharmacia, Uppsala, Sweden) with three density layers (1.076, 1.059, and 1.045 g/ml). The light fraction with predominantly monocytes was collected, washed, and seeded in 24-well or 6-well culture plates (Costar, Cambridge, MA, USA) at a density of 5 × 105 cells or 2,5 × 106 per well, respectively. After 60 min at 37°C, nonadherent cells were removed, and adherent cells were cultured to obtain immature DC in Iscove's modified Dulbecco's medium (IMDM; Life Technologies Ltd., Paisley, United Kingdom) with gentamicin (86 μg/ml; Duchefa, Haarlem, The Netherlands) and 10% fetal clone serum (HyClone, Logan, UT, USA) and supplemented with GM-CSF (500 U/ml; Schering-Plough, Uden, The Netherlands) and IL-4 (250 U/ml; Strathmann Biotec AG, Hannover, Germany). At day 3, the culture medium with supplements was refreshed. At day 6, maturation was induced by culturing the cells with poly (I:C) (20 μg/ml; Sigma-Aldrich, St. Louis, MO, USA). After two days, mature CD14- CD1b+ CD83+ DC were obtained. All subsequent tests were performed after harvesting and extensive washing of the cells to remove all factors. Mature DC were analysed for the expression of cell surface molecules by FACS. Mouse anti-human mAbs were used against the following molecules: CD14 (BD Biosciences, San Jose, CA, USA), CD1b (Diaclone, Besançon, France), CD83 (Immunotech, Marseille, France) and ICAM-1 (CD54) (Pelicluster, Sanquin, Amsterdam, The Netherlands). All mAb incubations were followed by incubation with FITC-conjugated goat F(ab')2 anti-mouse IgG and IgM (Jackson ImmunoResearch Laboratories, West Grove, PA, USA). Samples were analysed on a FACScan (BD Biosciences).
Peripheral Blood Leukocytes
Peripheral Blood Leukocytes (PBL) were isolated by layering PBMC from healthy donors and LAD-1 patients on a Percoll gradient. The heavy fraction with predominantly PBL was collected and stored at -150°C. PBL were cultured in IMDM with 10% FCS, gentamycin, 10 U/ml IL-2 (Cetus, Emeryville, CA, USA) and Staphylococcus enterotoxin B (SEB; Sigma-Aldrich; final concentration, 10 pg/ml). Mouse mAb to human CD28 (CLB-CD28/1) and human CD3 (CLB-T3/4E-1XE) were obtained from Sanquin (Amsterdam, The Netherlands).
C33A cervix carcinoma cells or PM1 T cells were transfected using calcium phosphate or electroporation respectively with 5 μg of the molecular clone of HIV-1 LAI. Since any of the patients could bear one or two mutant alleles for the CCR5 co-receptor, resulting is decreased susceptibility to CCR5-using HIV-1, we chose to use CXCR4-using HIV-1 LAI. The virus containing supernatant was harvested 3 to 5 days post transfection, filtered and stored at -80°C. The concentration of virus was determined by CA-p24 ELISA. C33A and PM1 cells were maintained in Dulbecco's Modified Eagle's Medium (DMEM) or Roswell Park Memorial Institute (RPMI) medium 1640 (Life Technologies) respectively, both supplemented with 10% FCS, 2 mM sodium pyruvate, 10 mM HEPES, 2 mM L-glutamine, penicillin (100 U/ml) (Sigma-Aldrich) and streptomycin (100 μg/ml) (Invitrogen, Breda, The Netherlands).
HIV transmission assay and CA-p24 measurement
Fully matured DC were incubated in a 96-well-plate (40–50 × 103 DC/50 μl/well) with PM1 produced virus (10 ng CA-p24/well) or C33A produced virus (20 ng) for 2 hr at 37°C. The DC were washed with PBS after centrifugation at 400 × g to remove unbound virus. Washing was repeated, followed by addition of 50 × 103 PBL. Prior to addition to DC the PBL were analyzed by FACS with the following mouse anti-human antibodies: FITC-labeled CD11a (Pelicluster, Sanquin), APC-labeled CD4 (BD Biosciences) and PE-labeled CXCR4 (BD Biosciences). CD18 (Pelicluster, Sanquin) incubation was followed by incubation with FITC-conjugated goat F(ab')2 anti-mouse IgG and IgM (Jackson ImmunoResearch Laboratories). Viral replication after transmission was followed by measuring CA-p24 in the culture supernatant by ELISA. To determine intracellular CA-p24 in the single-cycle transmission assay, saquinavir (Roche, London, United Kingdom at 0.2 μM) was added to prevent cell-to-cell spread of newly produced virions. After 48 hr, the cells were harvested and stained with FITC-labeled CD3 (BD Biosciences) and APC-labeled DC-SIGN (R7D Systems, MN, USA), followed by fixation with 4% PFA and washing with washing buffer (PBS with 2 mM EDTA and 0.5% BSA). Fixated cells were then washed with perm/wash buffer (BD Biosciences), and incubated with PE-labelled CA-p24 (KC57-RD1, Coulter, Hialeah, FL, USA) followed by washing with successively perm/wash- and washing buffer. Cells were then analysed by FACS.
Data were analysed for statistical significance (GraphPad InStat, Inc, San Diego, CA, USA) using ANOVA. A p value <0.05 was considered to be significant.
intercellular adhesion molecule-1
Leukocyte Adhesion Deficiency type 1
leukocyte function-associated molecule-1
Choi YK, Whelton KM, Mlechick B, Murphey-Corb MA, Reinhart TA: Productive infection of dendritic cells by simian immunodeficiency virus in macaque intestinal tissues. J Pathol. 2003, 201: 616-628. 10.1002/path.1482.
Hu J, Gardner MB, Miller CJ: Simian immunodeficiency virus rapidly penetrates the cervicovaginal mucosa after intravaginal inoculation and infects intraepithelial dendritic cells. J Virol. 2000, 74: 6087-6095. 10.1128/JVI.74.13.6087-6095.2000.
Spira AI, Marx PA, Patterson BK, Mahoney J, Koup RA, Wolinsky SM, Ho DD: Cellular targets of infection and route of viral dissemination after an intravaginal inoculation of simian immunodeficiency virus into rhesus macaques. J Exp Med. 1996, 183: 215-225. 10.1084/jem.183.1.215.
Banchereau J, Steinman RM: Dendritic cells and the control of immunity. Nature. 1998, 392: 245-252. 10.1038/32588.
Banchereau J, Briere F, Caux C, Davoust J, Lebecque S, Liu YJ, Pulendran B, Palucka K: Immunobiology of dendritic cells. Annu Rev Immunol. 2000, 18: 767-811. 10.1146/annurev.immunol.18.1.767.
Rowland-Jones SL: HIV: The deadly passenger in dendritic cells. Curr Biol. 1999, 9: R248-R250. 10.1016/S0960-9822(99)80155-9.
Pope M, Haase AT: Transmission, acute HIV-1 infection and the quest for strategies to prevent infection. Nat Med. 2003, 9: 847-852. 10.1038/nm0703-847.
Sanders RW, de Jong EC, Baldwin CE, Schuitemaker JH, Kapsenberg ML, Berkhout B: Differential transmission of human immunodeficiency virus type 1 by distinct subsets of effector dendritic cells. J Virol. 2002, 76: 7812-7821. 10.1128/JVI.76.15.7812-7821.2002.
McDonald D, Wu L, Bohks SM, KewalRamani VN, Unutmaz D, Hope TJ: Recruitment of HIV and its receptors to dendritic cell-T cell junctions. Science. 2003, 300: 1295-1297. 10.1126/science.1084238.
Groot F, van Capel TM, Kapsenberg ML, Berkhout B, de Jong EC: Opposing roles of blood myeloid and plasmacytoid dendritic cells in HIV-1 infection of T cells: transmission facilitation versus replication inhibition. Blood. 2006, 108: 1957-1964. 10.1182/blood-2006-03-010918.
Bromley SK, Burack WR, Johnson KG, Somersalo K, Sims TN, Sumen C, Davis MM, Shaw AS, Allen PM, Dustin ML: The immunological synapse. Annu Rev Immunol. 2001, 19: 375-396. 10.1146/annurev.immunol.19.1.375.
Dustin ML, Springer TA: T-cell receptor cross-linking transiently stimulates adhesiveness through LFA-1. Nature. 1989, 341: 619-624. 10.1038/341619a0.
van Kooyk Y, Kemenade W, Weder P, Kuijpers TW, Figdor CG: Enhancement of LFA-1-mediated cell adhesion by triggering through CD2 or CD3 on T lymphocytes. Nature. 1989, 342: 811-813. 10.1038/342811a0.
Springer TA: Adhesion receptors of the immune system. Nature. 1990, 346: 425-434. 10.1038/346425a0.
Hogg N, Bates PA: Genetic analysis of integrin function in man: LAD-1 and other syndromes. Matrix Biol. 2000, 19: 211-222. 10.1016/S0945-053X(00)00066-4.
Anderson DC, Springer TA: Leukocyte adhesion deficiency: an inherited defect in the Mac-1, LFA-1, and p150,95 glycoproteins. Annu Rev Med. 1987, 38: 175-194. 10.1146/annurev.me.38.020187.001135.
Springer TA: Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm. Cell. 1994, 76: 301-314. 10.1016/0092-8674(94)90337-9.
Lawrence MB, Springer TA: Leukocytes roll on a selectin at physiologic flow rates: distinction from and prerequisite for adhesion through integrins. Cell. 1991, 65: 859-873. 10.1016/0092-8674(91)90393-D.
von Andrian UH, Chambers JD, McEvoy LM, Bargatze RF, Arfors KE, Butcher EC: Two-step model of leukocyte-endothelial cell interaction in inflammation: distinct roles for LECAM-1 and the leukocyte beta 2 integrins in vivo. Proc Natl Acad Sci U S A. 1991, 88: 7538-7542. 10.1073/pnas.88.17.7538.
Kuijpers TW, van Lier RA, Hamann D, de Boer M, Thung LY, Weening RS, Verhoeven AJ, Roos D: Leukocyte adhesion deficiency type 1 (LAD-1)/variant. A novel immunodeficiency syndrome characterized by dysfunctional beta2 integrins. J Clin Invest. 1997, 100: 1725-1733.
Diamond MS, Springer TA: The dynamic regulation of integrin adhesiveness. Curr Biol. 1994, 4: 506-517. 10.1016/S0960-9822(00)00111-1.
van Kooyk Y, Figdor CG: Avidity regulation of integrins: the driving force in leukocyte adhesion. Curr Opin Cell Biol. 2000, 12: 542-547. 10.1016/S0955-0674(00)00129-0.
Wlodawer A, Vondrasek J: Inhibitors of HIV-1 protease: a major success of structure-assisted drug design. Annu Rev Biophys Biomol Struct. 1998, 27: 249-284. 10.1146/annurev.biophys.27.1.249.
Ganesh L, Leung K, Lore K, Levin R, Panet A, Schwartz O, Koup RA, Nabel GJ: Infection of specific dendritic cells by CCR5-tropic human immunodeficiency virus type 1 promotes cell-mediated transmission of virus resistant to broadly neutralizing antibodies. J Virol. 2004, 78: 11980-11987. 10.1128/JVI.78.21.11980-11987.2004.
Shamri R, Grabovsky V, Gauguet JM, Feigelson S, Manevich E, Kolanus W, Robinson MK, Staunton DE, von Andrian UH, Alon R: Lymphocyte arrest requires instantaneous induction of an extended LFA-1 conformation mediated by endothelium-bound chemokines. Nat Immunol. 2005, 6: 497-506. 10.1038/ni1194.
Ingulli E, Mondino A, Khoruts A, Jenkins MK: In vivo detection of dendritic cell antigen presentation to CD4(+) T cells. J Exp Med. 1997, 185: 2133-2141. 10.1084/jem.185.12.2133.
Steinman RM: The dendritic cell system and its role in immunogenicity. Annu Rev Immunol. 1991, 9: 271-296. 10.1146/annurev.iy.09.040191.001415.
Atarashi K, Hirata T, Matsumoto M, Kanemitsu N, Miyasaka M: Rolling of Th1 cells via P-selectin glycoprotein ligand-1 stimulates LFA-1-mediated cell binding to ICAM-1. J Immunol. 2005, 174: 1424-1432.
Carman CV, Springer TA: Integrin avidity regulation: are changes in affinity and conformation underemphasized?. Curr Opin Cell Biol. 2003, 15: 547-556. 10.1016/j.ceb.2003.08.003.
van Kooyk Y, van Vliet SJ, Figdor CG: The actin cytoskeleton regulates LFA-1 ligand binding through avidity rather than affinity changes. J Biol Chem. 1999, 274: 26869-26877. 10.1074/jbc.274.38.26869.
Hogg N, Henderson R, Leitinger B, McDowall A, Porter J, Stanley P: Mechanisms contributing to the activity of integrins on leukocytes. Immunol Rev. 2002, 186: 164-171. 10.1034/j.1600-065X.2002.18614.x.
Constantin G, Majeed M, Giagulli C, Piccio L, Kim JY, Butcher EC, Laudanna C: Chemokines trigger immediate beta2 integrin affinity and mobility changes: differential regulation and roles in lymphocyte arrest under flow. Immunity. 2000, 13: 759-769. 10.1016/S1074-7613(00)00074-1.
Cairo CW, Mirchev R, Golan DE: Cytoskeletal Regulation Couples LFA-1 Conformational Changes to Receptor Lateral Mobility and Clustering. Immunity. 2006, 25: 297-308. 10.1016/j.immuni.2006.06.012.
Porter JC, Bracke M, Smith A, Davies D, Hogg N: Signaling through integrin LFA-1 leads to filamentous actin polymerization and remodeling, resulting in enhanced T cell adhesion. J Immunol. 2002, 168: 6330-6335.
Arrighi JF, Pion M, Garcia E, Escola JM, van Kooyk Y, Geijtenbeek TB, Piguet V: DC-SIGN-mediated infectious synapse formation enhances X4 HIV-1 transmission from dendritic cells to T cells. J Exp Med. 2004, 200: 1279-1288. 10.1084/jem.20041356.
Fortin JF, Cantin R, Tremblay MJ: T cells expressing activated LFA-1 are more susceptible to infection with human immunodeficiency virus type 1 particles bearing host-encoded ICAM-1. J Virol. 1998, 72: 2105-2112.
Hioe CE, Chien PC, Lu C, Springer TA, Wang XH, Bandres J, Tuen M: LFA-1 expression on target cells promotes human immunodeficiency virus type 1 infection and transmission. J Virol. 2001, 75: 1077-1082. 10.1128/JVI.75.2.1077-1082.2001.
Tardif MR, Tremblay MJ: Presence of host ICAM-1 in human immunodeficiency virus type 1 virions increases productive infection of CD4+ T lymphocytes by favoring cytosolic delivery of viral material. J Virol. 2003, 77: 12299-12309. 10.1128/JVI.77.22.12299-12309.2003.
Tardif MR, Tremblay MJ: Regulation of LFA-1 Activity through Cytoskeleton Remodeling and Signaling Components Modulates the Efficiency of HIV Type-1 Entry in Activated CD4+ T Lymphocytes. J Immunol. 2005, 175: 926-935.
Tsunetsugu-Yokota Y, Yasuda S, Sugimoto A, Yagi T, Azuma M, Yagita H, Akagawa K, Takemori T: Efficient virus transmission from dendritic cells to CD4+ T cells in response to antigen depends on close contact through adhesion molecules. Virol. 1997, 239: 259-268. 10.1006/viro.1997.8895.
Bounou S, Giguere JF, Cantin R, Gilbert C, Imbeault M, Martin G, Tremblay MJ: The importance of virus-associated host ICAM-1 in human immunodeficiency virus type 1 dissemination depends on the cellular context. FASEB J. 2004, 18: 1294-1296.
Weitz-Schmidt G, Welzenbach K, Brinkmann V, Kamata T, Kallen J, Bruns C, Cottens S, Takada Y, Hommel U: Statins selectively inhibit leukocyte function antigen-1 by binding to a novel regulatory integrin site. Nat Med. 2001, 7: 687-692. 10.1038/89058.
Giguere JF, Tremblay MJ: Statin compounds reduce human immunodeficiency virus type 1 replication by preventing the interaction between virion-associated host intercellular adhesion molecule 1 and its natural cell surface ligand LFA-1. J Virol. 2004, 78: 12062-12065. 10.1128/JVI.78.21.12062-12065.2004.
Anderson ME, Siahaan TJ: Targeting ICAM-1/LFA-1 interaction for controlling autoimmune diseases: designing peptide and small molecule inhibitors. Peptides. 2003, 24: 487-501. 10.1016/S0196-9781(03)00083-4.
Liu G, Huth JR, Olejniczak ET, Mendoza R, DeVries P, Leitza S, Reilly EB, Okasinski GF, Fesik SW, von Geldern TW: Novel p-arylthio cinnamides as antagonists of leukocyte function-associated antigen-1/intracellular adhesion molecule-1 interaction. 2. Mechanism of inhibition and structure-based improvement of pharmaceutical properties. J Med Chem. 2001, 44: 1202-1210. 10.1021/jm000503f.
Shimaoka M, Salas A, Yang W, Weitz-Schmidt G, Springer TA: Small molecule integrin antagonists that bind to the beta2 subunit I-like domain and activate signals in one direction and block them in the other. Immunity. 2003, 19: 391-402. 10.1016/S1074-7613(03)00238-3.
This research has been funded by grant 7008 from Aids Fonds Netherlands. We thank Rogier Sanders for critical reading of the manuscript.