- Research article
- Open Access
Antibodies to the CD4-binding site of HIV-1 gp120 suppress gp120-specific CD4 T cell response while enhancing antibody response
© Visciano et al; licensee BioMed Central Ltd. 2008
- Received: 21 April 2008
- Accepted: 18 July 2008
- Published: 18 July 2008
The binding of Abs to the CD4-binding site (CD4bs) of HIV-1 envelope gp120 has been shown to obstruct the processing and generation of helper epitopes from this antigen, resulting in poor presentation of various gp120 epitopes by MHC class II to CD4 T cells. However, the physiologic significance of these inhibitory anti-CD4bs Abs in vivo has remained unclear. In this study, we evaluated the immunologic effects of anti-CD4bs Abs in vivo using a murine model.
Animals were immunized with recombinant envelope proteins with or without CD4-binding activity (designated CD4bs+ Env and CD4bs– Env, respectively). As expected, anti-CD4bs Abs were generated only after immunization with CD4bs+ Env and not with CD4bs– Env. The presence of anti-CD4bs Abs was associated with lower levels of envelope-specific lymphoproliferation in animals immunized with CD4bs+ Env. To further determine the specific role of the anti-CD4bs Abs, we immunized mice with gp120 in the presence of an inhibitory anti-CD4bs mAb or a non-inhibitory anti-gp120 mAb. The data show that the presence of anti-CD4bs mAb reduced CD4 T cell responses to gp120. However, we also detected significantly higher titers of anti-gp120 Abs following immunization with gp120 and the anti-CD4bs mAb.
Anti-CD4bs Abs can exert discordant effects on the gp120-specific CD4 T cell and Ab responses in vivo, indicating the importance of these particular Abs in influencing both the cellular and the humoral immune responses against HIV-1.
- Peptide Pool
- Lymphoproliferative Response
- Gp120 Antigen
- Envelope Antigen
- Helper Epitope
The capacity of antibodies (Abs) to enhance or decrease antigen presentation for MHC class II-restricted CD4 T cells is well documented in the literature [1–7]. Our previous studies have demonstrated that MHC class II presentation of HIV-1 gp120 is abrogated when this antigen is bound by monoclonal Abs (mAbs) to the CD4-binding site (CD4bs) of gp120 [1, 2, 8]. This effect is specific for the anti-CD4bs Abs, since the other mAbs directed to other regions of gp120 cause no significant inhibition. Interestingly, inhibitory anti-CD4bs mAbs are commonly produced by chronically HIV-1-infected subjects [9, 10]; these mAbs have high affinity for gp120 but poor or no neutralizing activity against primary HIV-1 isolates [8, 11]. Low affinity anti-CD4bs Abs generated upon limited exposure to gp120, either during acute infection or after a short course of immunization, are not inhibitory, whereas the exceptional anti-CD4bs IgG1 b12 that mediates potent and broad virus-neutralizing activity causes only partial inhibition ( and Hioe et al. unpublished data).
The mechanisms by which anti-CD4bs mAbs inhibit gp120 antigen presentation to CD4 T cells have been previously investigated. Upon binding to gp120, the inhibitory anti-CD4bs mAbs do not affect gp120 uptake or transport into the acidic endolysosomes of antigen-presenting cells [8, 12]. These mAbs and gp120/mAb complexes also do not directly affect the CD4 T cells. The T cells remain responsive to synthetic peptides representing already-processed gp120 epitopes, and CD4 T cells specific for other antigens, such as HIV-1 p24, Mycobacterium tuberculosis MPT-32 and 85C, and cytomegalovirus, are not affected by the mAbs or immune complexes. Instead, upon the uptake of the gp120/anti-CD4b Ab complexes by antigen-presenting cells into the endolysosomal compartments, the complexes remain quite stable at the acidic pH of the endolysosomes  and are resistant to proteolytic digestion by endolysosomal enzymes [8, 12]. Taken together, these data support the notion that the binding of mAbs to the CD4bs obstructs gp120 proteolytic processing by antigen-presenting cells such that peptidic helper epitopes are not efficiently generated and presented on MHC class II to CD4 T cells.
It should be noted, however, that the obstructive effect of the anti-CD4bs mAbs is not simply due to steric hindrance or masking of a particular helper epitope by the mAbs. These mAbs inhibit the processing and presentation of all gp120 epitopes examined thus far, including those in the C1, C2, V2, or V3 regions , indicative of their global effects. Importantly, the helper epitopes are located at sites distant from or irrelevant for the binding sites of the anti-CD4bs mAbs. These findings corroborate previously reported data of Kwong et al  indicating that the binding of mAbs to the CD4bs, but not to other gp120 regions, induces a large entropy change in gp120, causing an overall increase in gp120 resistance to enzymatic degradation. The entropic change is also accompanied by structural and antigenic alterations as evidenced by significant increases of the mAb reactivity to the V3 loop and the N terminus of gp120 when gp120 is bound by the anti-CD4bs mAbs . The thermodynamic and antigenic changes induced by anti-CD4bs mAbs can be explained by the structural data showing that, unlike most Abs which bind epitopes located in one particular domain of a protein, e.g. the V3 loop in gp120 [15–17], the anti-CD4bs mAbs, similar to CD4 and the CD4i mAbs specific for the chemokine receptor binding site, draw together both the inner and outer domains of gp120 and bind to a surface that is formed by both of these domains [13, 18–21].
While the capacity of anti-CD4bs Abs to block MHC class II presentation and CD4 T cell responses to gp120 has been demonstrated in vitro with human CD4 T cell lines or clones [1, 2, 8, 12], the in vivo effects of the anti-CD4bs Abs have yet to be investigated. The present study has been designed to examine the physiologic activities of anti-CD4bs Abs in vivo using a murine model. Specifically, we asked whether the presence of anti-CD4bs Abs in vivo affects the induction of envelope-specific cellular responses and if the alterations also influence the Ab responses to this antigen. To answer these questions, we initially compared the immunogenicity of envelope antigens that have or do not have CD4-binding activity. Subsequently, we performed in vitro and in vivo studies to test the specific role of anti-CD4bs Abs. The data from these studies demonstrate that the presence of anti-CD4bs mAbs reduces lymphoproliferative responses to gp120 in vivo as well as in vitro. However, the reduced cellular responses do not lead to diminished Ab responses to gp120; the anti-gp120 Ab levels are actually augmented in animals immunized with gp120 in the presence of an anti-CD4bs mAb.
Immunization with envelope antigen lacking the CD4 binding site stimulates higher levels of envelope-specific T cell responses
Ab levels to whole gp120 and to CD4bs in sera of mice immunized with envelope proteins that have or lack CD4 binding activitya
No Ag & IFA
CD4bs+ Env & IFA
CD4bs- Env & IFA
No Ag & RIBI
CD4bs+ Env & RIBI
CD4bs- Env & RIBI
> 12500 (12500->12500)
Monoclonal anti-CD4bs Abs suppress gp120 antigen presentation to mouse CD4 T cells
Immunization with the gp120/anti-CD4bs Ab complex induces a lower gp120-specific lymphoproliferative response
To determine if there are any alterations in the epitopes recognized by mice immunized with the gp120/anti-CD4bs complex, splenocytes were tested for recognition of 20-mer overlapping peptide pools encompassing the entire gp120. Each pool contained six different peptides representing a particular region of gp120, i.e. C1 (pool 1), C1-V1 (pool 2), V2 (pool 3), C2 (pool 4), C2-V3 (pool 5), C3-V4 (pool 6), V4-C4 (pool 7), and C5 (pool 8) and was tested at the final concentration of 1 μg/ml for each peptide. The results showed that in all groups of mice the highest lymphoproliferative response was directed to peptide pool 1 which represents the C1 region of gp120 (Fig. 3B). However, similar to the response to the whole gp120 protein, the anti-C1 response of mice that received the gp120/654 mAb complex was lower than those of the other two groups. The mice immunized with the gp120/654 complex also did not display significant proliferative responses to any other peptide pools tested, while the other groups showed recognition of peptide pools 3, 4, and 5, which encompass the V2 to V3 regions of gp120. Mice immunized with adjuvant only did not show any reactivity with the peptide pools (SI < 2 with each pool). These results indicate that the anti-CD4bs Abs suppress the induction of CD4 T cell responses to various epitopes on gp120, consistent with the global suppressive effects of these Abs on the processing and generation of all gp120 epitopes examined to date [1, 2]. Taken together, the data indicate that the presence of Abs to the CD4-binding site of gp120 negatively affects the generation of gp120-specific lymphoproliferative responses in vivo, similar to the suppression seen in vitro on the responses of established murine and human gp120-specific CD4 T cell clones or lines.
The presence of anti-CD4bs mAbs enhances the Ab response to gp120
This study provides the first in vivo evidence that the presence of Abs to the CD4bs of gp120 alters CD4 T cell and Ab responses to the gp120 antigen in disparate ways. These effects were specifically observed with anti-CD4bs Abs, and not with other anti-gp120 Abs examined. Hence, higher envelope-specific lymphoproliferation was induced in mice immunized with an envelope protein that lacks the CD4-binding activity and cannot elicit anti-CD4bs Abs. By contrast, lymphoproliferative responses to gp120 were lower when mice were immunized with gp120 in complex with an anti-CD4bs mAb as compared to uncomplexed gp120 or gp120 complexed with a different mAb. These data are consistent with in vitro data shown in Fig. 2 with a mouse CD4 T cell clone and with previously published results with a number of human CD4 T cell lines [1, 2, 8, 12] demonstrating that the CD4 T cell proliferative responses to gp120 are suppressed in the presence of anti-CD4bs mAbs, but not other anti-gp120 or control mAbs. However, the diminished levels of gp120-specific lymphoproliferation induced in mice receiving gp120 and anti-CD4bs Abs are not accompanied by the corresponding reduction of Ab levels to gp120. As indicated by faster kinetics and higher Ab titers (Fig. 4 and , the Ab response to gp120 was actually enhanced in mice immunized with the gp120/anti-CD4bs complex. The enhanced Ab levels were seen in the sera with gp120-specific IgG as well as IgA, but not IgM (Fig. 4 and ). Moreover, we previously reported that the anti-gp120 Abs produced by immunization with the gp120/anti-CD4bs Ab complex were mainly of the IgG1 subclass , indicating the capacity of the anti-CD4bs Abs to skew anti-gp120 immune responses toward the Th2-type response.
Our earlier studies showed that the suppressive effects of the anti-CD4bs Abs on MHC class II presentation of gp120 antigen required a molar Ab/gp120 of at least 1 , indicating that formation of immune complexes is essential for suppression. Specifically, the gp120/anti-CD4bs complexes were found to be more resistant to endolysosomal proteases and other degradative enzymes, such as Endo H, than gp120 alone or gp120 complexed with mAbs to the C terminus, N terminus, or the variable loops [8, 12, 13]. Since CD4 T cells recognize proteolytically processed antigens, it stands to reason that the gp120/anti-CD4bs mAb complexes are poor immunogens for the CD4 T cells. Conversely, the protease-resistant gp120/anti-CD4bs complexes may serve as a more durable antigen source for B cells that recognize intact unprocessed antigens, leading to enhanced production of Abs against gp120. It should also be noted that the binding of Abs to the CD4bs of gp120 has been shown to alter gp120 antigenicity such that Ab reactivity to the specific regions of gp120, including C1 and V3, is significantly enhanced [14, 27]. Consistent with these data, we observed that the enhanced Ab responses induced in mice receiving the gp120/anti-CD4bs complexes were primarily directed to the V3 loop, whereas the Ab levels to the gp120 core lacking C1, V1/V2, V3, and C5 were not increased .
The capacity of anti-CD4bs Abs to suppress gp120 antigen presentation to CD4 T cells while enhancing and redirecting the Ab response to the V3 loop indicates the potential role of these Abs in HIV-1 immunopathogenesis, although further studies are required to examine this issue. Studies from our lab as well as others have shown that, except for recombinant anti-CD4bs IgG b12, anti-CD4bs Abs naturally produced during HIV infection have little or no neutralizing activity against most HIV-1 primary isolates [19, 28]. Hence, induction of these Abs is not likely to offer much protection against the virus. Instead, the formation of gp120/anti-CD4bs complexes during HIV-1 infection may actually contribute to further suppression of anti-viral CD4 T cell responses. Moreover, our previous studies demonstrate that Ab responses induced by these complexes were skewed toward strain-specific epitopes on the V3 loop and away from the more conserved epitopes on V3 [14, 29]. Due to steric hindrance or structural alterations induced upon Ab binding to the CD4bs, the presence of these poorly neutralizing anti-CD4bs Abs also prevented the generation of more potent and cross-reactive Abs to the CD4bs or the chemokine receptor binding site .
Among HIV-1 infected subjects, anti-CD4bs Abs were predominantly found in the sera of progressors, while no or very low levels of these Abs were detected in long-term non-progressors or elite controllers . Among the progressors, significantly higher levels of the anti-CD4bs Abs were produced by rapid progressors (with declining CD4 counts of > 53 cells/mm3/6 months) prior to development of AIDS than by slow progressors (with no CD4 decline in 7 years of follow-up) . Notably, chronically HIV-1 infected progressors do not display significant CD4 T cell responses to envelope antigens [30, 31]. Only a small percentage of HIV-1 infected subjects are able to maintain their envelope-specific lymphoproliferation; some of these subjects are long-term non-progressors and some are chronic or acute patients who received anti-retroviral therapy . However, regardless of their clinical status, these exceptional individuals have undetectable or low levels of serum anti-CD4bs Abs, similar to long-term non-progressors and elite controllers. Hence, consistent with the data from the immunized mice, the presence of anti-CD4bs Abs in HIV-1-infected subjects is associated with the lack of envelope-specific CD4 T cell responses. On the other hand, CD4 T cell responses to envelope may be maintained in the absence of these Abs. It should also be noted that all of the rare HIV+ subjects with envelope-specific lymphoproliferation produce very low serum Ab titers to the whole gp120 antigen (geomean half max of 130 with a range of < 25–1500) as compared to slow or rapid progressors (geomean half max of 1500 and 1700, respectively)  demonstrating the discordance between CD4 T cell and Ab responses to envelope in HIV-1-infected subjects, similar to that seen in the immunized mice. By contrast, the anti-p24 Ab titers are higher in most subjects with envelope-specific lymphoproliferation than in progressors, indicating that the inverse association between CD4 T cell and Ab responses is specific for envelope.
Although a discordance between CD4 T cell and Ab responses to envelope was rather surprising, these findings are consistent with recent studies on chronic lymphocytic choriomeningitis virus (LCMV) infection in mice demonstrating that partial removal or tolerization of virus-specific CD4 T cell responses actually enhanced anti-viral Ab responses [32, 33]. Likewise, blocking of CD27-mediated signaling on CD4 T cells to prevent the secretion of IFN-γ and TNF-α, elicited neutralizing Ab responses against LCMV and reduced virus burden . One explanation proposed to explain this phenomenon is that high levels of inflammatory cytokines produced by T cells, including IFN-γ and TNF-α, during a chronic virus infection causes lymphoid tissue damage and retards the capacity of B cells to produce high-affinity Abs effective against the virus. Nevertheless, the loss of CD4 T cell responses during a chronic LCMV infection was also shown to result in the failure to mount Ab responses to escape variants, indicating that a proper balance between CD4 T cell and Ab responses is crucial for effective anti-viral immunity. Another possibility is that rather than the quantity, it is the quality of the CD4 T cell responses which determines the optimal anti-viral Ab responses, although the specific quality or functions required remain unclear.
In summary, we have demonstrated that the binding of Abs to the CD4bs have distinct effects on CD4 T cell and Ab responses to HIV-1 envelope antigen in vivo. These modulating activities correspond with the capacity of the particular Abs to alter structural conformation and proteolytic processing of the envelope antigen. A better understanding about the interaction between Ab reactivity and CD4 T cell recognition of HIV-1 antigens is needed for developing more effective vaccines against the virus.
BALB/c or B10.A mice (female, > 6 weeks old from Jackson Lab) were immunized as previously described . In brief, mice were inoculated i.p. with envelope antigens, alone or with the designated mAb. MPL+TDM (Ribi) or incomplete Freund's adjuvant (IFA) (Sigma-Aldrich, St Louis, MO) were used as adjuvants. When gp120 and mAb were used as immunogens, the immune complexes were prepared by incubating gp120 with the mAb for 2 hrs at 37°C, and then mixed with Ribi adjuvant. Animals were immunized 4 or 5 times at the designated intervals followed by collection of blood and spleens. The animal studies were carried out according to a protocol approved by the VA and NYU IACUC.
T cell proliferation was assessed using a standard 3H-thymidine incorporation assay. To evaluate T cell responses in immunized mice, freshly isolated splenocytes were resuspended in complete RPMI medium supplemented with 2.5% IgG-depleted FBS or with 10% FBS. The cells were then incubated at a concentration of 3 × 105/well either with antigen or with medium alone for 5 days. The cells were pulsed with 3H-thymidine for 16–22 hr prior to harvest. Each experimental condition was tested in six replicates.
The gp120-specific mouse CD4 T cell clone T1 was tested for proliferative response as described previously . Irradiated mouse splenocytes used as APCs were treated with gp120 or gp120 complexed with anti-gp120 mAbs, and incubated with the T cell clone. T cell responses to APCs alone in the absence of any antigen were determined in each assay as background proliferation. Each experimental condition was tested in triplicate and all experiments were performed at least twice.
ELISA for detection of serum Abs
Ig subtypes of gp120-specific Abs in the sera were detected by ELISA as previously described . Briefly, ELISA plates (Immunoblot 2HB Thermo, Milford, MA) were coated with 1 μg/ml sheep polyclonal anti-C5 Ab (Cliniqa, Fallbrook, CA) to capture gp120LAI (1 μg/ml). Sera were then reacted for 2 hrs at 37°C. Rabbit Abs against mouse IgG or IgM (Zymed, San Francisco, CA) were added, and alkaline phosphatase-conjugated goat anti-rabbit IgG (Sigma-Aldrich, Saint Louis, MO) was used as a secondary Ab and p-nitrophenyl phosphate (Sigma-Aldrich, Saint Louis, MO) was used as the substrate.
ELISA used to detect anti-CD4bs serum Ab was described previously . Briefly, gp120IIIB was captured onto the plate by sheep polyclonal anti-C5 Ab, washed, and reacted with sera. Soluble human CD4 (Progenics) was then added, and bound CD4 was detected using a mouse anti-human CD4 MAb OKT4 and goat anti-mouse IgG Abs conjugated to alkaline phosphatase. Each sample was tested in duplicate wells at least twice.
We thank Drs. J. Ahler and J. Berzofsky (National Institutes of Health) for the mouse CD4 T cell clone, Drs. M. K. Gorny and S. Zolla-Pazner (New York University- School of Medicine) for the mAbs, and Dr. Jennifer Fuller for editing the manuscript.
The work was supported by a Merit Review Award and the Research Enhancement Award Program of the U.S. Department of Veterans Affairs, the New York University Center for AIDS Research Immunology Core (AI-27742), and by NIH grant AI-48371.
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