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Topical microbicides are a leading strategy for prevention of HIV mucosal infection to women, however, numerous pharmacokinetic limitations associated with coitally-related dosing strategy have contributed to their limited success. Here we test the hypothesis that adeno-associated virus (AAV) mediated delivery of the b12 human anti-HIV-1 gp120 minibody gene to the lower genital tract of female rhesus macaques (Rh) can provide prolonged expression of b12 minibodies in the cervical-vaginal secretions. Gene transfer studies demonstrated that, of various GFP-expressing AAV serotypes, AAV-6 most efficiently transduced freshly immortalized and primary genital epithelial cells (PGECs) of female Rh in vitro. In addition, AAV-6-b12 minibody transduction of Rh PGECs led to inhibition of SHIV162p4 transmigration and virus infectivity in vitro. AAV-6-GFP could also successfully transduce vaginal epithelial cells of Rh when applied intra-vaginally, including p63+ epithelial stem cells. Moreover, intra-vaginal application of AAV-6-b12 to female Rh resulted in prolonged minibody detection in their vaginal secretions throughout the 79 day study period. These data provide proof-of-principle that AAV-6-mediated delivery of anti-HIV broadly neutralizing antibody (BnAb) genes to the lower genital tract of female Rh results in persistent minibody detection for several months. This strategy offers promise that an anti-HIV-1 genetic microbicide strategy may be possible in which topical application of AAV vector, with periodic reapplication as needed, may provide sustained local BnAb expression and protection.
Women are at much higher risk of acquiring HIV-1 infection through heterosexual transmission than men, and constitute more than half of all HIV/AIDS cases worldwide.1 While the mucosal lining of the female genital tract usually presents a robust barrier against pathogens via a variety of physical and immunologic defenses, the specific roles that vaginal, ectocervical and endocervical mucosa play in protection against HIV-1 transmission remains unknown. The stratified squamous epithelium of the vaginal and ectocervical mucosa is alleged to provide better mechanical protection against pathogens compared to the single layer columnar epithelium of the endocervix2, although recent observations have suggested otherwise.3 HIV-1 transmission can also occur across the vaginal/ectocervical epithelia as well as the cervical transformation zone.4-6 Langerhan's cells reside close to the surface of vaginal and ectocervical mucosae and may transfer HIV-1 to CD4+ T cells that normally reside below the epithelial layer. Epithelial cells also secrete several biological factors that can inhibit HIV infection and migration 7-12. Damage or disruption of the epithelial layer increases the ability of HIV-1 to penetrate the mucosal layer and allows HIV-1 virions to access to cell types permissive for infection.13, 14 This process is thought to be essential for HIV-1 to establish infection as the genital epithelial cells themselves lack CD4 receptors.
In addition to an effective vaccine to protect against HIV infection, development of a potent anti-HIV microbicide remains an important strategy to prevent HIV transmission. However, to date, six candidate microbicides have been found to be ineffective in phase IIb or III clinical trials.15-22 The CAPRISA 004 phase IIb trial provided proof of concept for vaginal microbicides, demonstrating that 1% tenofovir microbicide gel reduced the risk of HIV acquisition for women by 39% overall, and by 54% in women reporting >80% adherence to the dosing regimen15, 23, yet another clinical trial of one-daily dosing regimen with tenofovir gel failed to demonstrate any detectable efficacy in at risk women24. These studies underline the need to develop additional microbicide strategies with complementary or synergistic activity 25. Equally important is the recognition that patient adherence to microbicide dosing regimens is critical to reducing the risk of HIV acquisition, particularly when an effective microbicide is available.26
The recent identification of novel highly potent human anti-HIV broadly neutralizing antibodies (BnAbs) and their further improvement by structure based design has led to intense interest in their possible use in pre-exposure prophylaxis.27, 28 In addition, in the absence of an effective vaccine, vector mediated gene transfer has received renewed interest as an immunoprophylaxis strategy to engineer secretion of existing BnAbs into the circulation.29-31 Adeno-associated virus (AAV) vectors are particularly attractive for therapeutic antibody (Ab) gene delivery29, 31 because of their safety and efficacy profile32, 33 and the ability of different serotypes to transduce a variety of tissue and cell types.33 Furthermore, transduction is potentially long lasting, directing gene expression over a period of months to years in non-dividing tissues.31, 33, 34 For example, persistent neutralizing activity was seen for at least 24 weeks following a single intramuscular injection of AAV encoding the prototypic human anti-HIV-1 gp120 CD4 binding site (CD4BS) BnAb, b12, into mouse muscle.35 More recently, similar delivery of further engineered self-complementary AAV (scAAV) vector encoding b12 IgG in humanized mice provided protection from infection when challenged intravenously or intravaginally with HIV-1.29, 36 In addition, we have previously demonstrated AAV vectors encoding b12 IgG1 minibodies (bivalent single chain antibody (scFv) with Fc, (scFvFc)) can transduce human primary genital epithelial cells (PGECs) and their stem cells in vitro and block HIV-1 transmigration and infection.37 This Ab format was chosen for ease of cloning, high levels of expression, maintenance of Fc effector functions and potential greater tissue penetration than IgGs due to their smaller size. Transduction of epithelial stem cells is expected to be a key feature of persistence, as the apical layers of the cervical-vaginal mucosa continuously sheds whereas the basal layers of the mucosa including the epithelial stem cells is maintained as a replenishing source of squamous epithelial cells. Whether persistent minibody expression from the transduced stem cell population will be for years is not known however, even if gradual diminishing expression from the extrachromosomal AAV vector occurs over time, therapeutically meaningful local concentrations of anti-BnAbs may still be expressed for several months. Indeed, the use of AAV vectors for gene transfer to lung epithelial cells38 and their progenitors39, 40 as well as other stem cell types41-43 has recently been demonstrated.
The rhesus macaque (Macaca mulatta) (Rh) model is used extensively as a surrogate for testing HIV-1 microbicides because of the many similarities between the anatomy and physiology of the human and primate genital tracts.44, 45 In the present study, we evaluated multiple AAV serotypes for gene transfer to freshly immortalized endo- and ecto-cervical and vaginal epithelial cell lines derived from female Rh and Rh PGECs. We performed pilot AAVGFP gene transfer studies to the lower genital track of female Rh to evaluate the feasibility of stem cell gene transfer and duration of transgene expression. We also modified our procedures for AAV-gene transfer to include scarification of the cervical-vaginal epithelium to better expose the basal epithelial stem cell layer. For these studies, we chose AAV-encoding b12-scFvFc minibodies as b12 IgG effectively neutralizes the chimeric R5 tropic virus SHIV162p4 in vitro46 and protects macaques against vaginal challenge with SHIV162p4 following Ab application to the cervical-vaginal mucosa46 Our results show that intra-vaginal application of AAV-6-b12 vector to female Rh resulted in sustainable detection of b12 minibodies in vaginal secretions for at least several months. AAV-anti-HIV BnAb gene transfer to the vaginal and cervical epithelium stem cell compartment represents a novel microbicide strategy that may, with further optimization, have potential for preventing HIV-1 infection in women during heterosexual transmission.
Papillomavirus-immortalized cell lines from normal human vaginal, ecto- and endo-cervical cells have been previously generated and cultured for in vitro studies.47, 48 These cell lines maintain expression of tissue-specific differentiation proteins and were similar to primary organotypic cultures.48 To evaluate transduction of corresponding Rh macaque tissues by AAV vectors, we generated immortalized Rh/V/E6E7, Rh/Ect/E6E7 and Rh/End/E6E7 cell lines from healthy Rh macaque vaginal, ecto- and endo-cervical epithelia, respectively using retroviral vector LXSN-16E6E7 transduction.48 A representative example of the immortalized vaginal cell line morphology in culture is shown in Figure 1A, in which small keratinocyte-like cells are observed by light microscopy (panel b), in contrast to the primary cell cultures (panel a). In Ca2+-supplemented (0.4 mM CaCl2) keratinocyte serum-free medium, the immortalized cells formed tight colonies of attached sister cells (panels c-d) and the doubling time of the cultures was approximately 72 hrs. The Rh immortalized vaginal epithelial cell line Rh/V/E6E7 closely resembled the corresponding human immortalized vaginal cell line hu/V/E6E7 (Figure 1A, panels e-f). The immortalized cell lines were then stained with monoclonal antibodies specific for epithelial cell markers including, cytokeratin (ck) 19, 10 and 18 as well as secretory component (SC). As summarized in Table 1, Rh/V/E6E7, Rh/Ect/E6E7 and Rh/End/E6E7 cell lines stained positive for expression of ck19. In contrast, the Rh/End/E6E7 cell line did not stain positive for ck10 and Rh/V/E6E7 cell line was negative for ck18 staining. Thus, positive staining for ck19 and differential negative staining for ck10 and ck18 could be used to distinguish the three cell lines. Figure 1B shows representative positive staining of the immortalized vaginal epithelial cell line Rh/V/E6E7 for ck19 and ck10.
Due to the fact that different AAV serotypes differentially transduce a wide variety of cells and tissues, 8 different AAV serotypes were evaluated to determine the optimal serotype(s) that most efficiently transduced female Rh genital epithelial cells. The transduction efficiencies of GFP-expressing AAV-1, 2, 3, 4, 5, 6, 8 and 9 (at multiplicity of infection (MOI) of 2×105 viral genome (vg) per cell) were evaluated on the three immortalized Rh cell lines. Expression of GFP protein was detected by flow cytometry and was represented as percentage of GFP positive cells (Figure 2A). GFP expression was also assessed visually by fluorescence microscopy (Figure 2B). All cell lines were successfully transduced with AAV-1, AAV-2, AAV-5 and AAV-6, with the most efficient transduction occurring with AAV-2 and AAV-6. In contrast, transduction efficiencies of serotypes AAV-3, AAV-4, AAV-8 and AAV-9 were low in these cell lines. To confirm that the inability of AAV-8 and AAV-9 to transduce Rh macaque female genital cell lines was due to their tropism for the specific cell type, and not to a defect in the vectors themselves, COS-1 cells were tested for transduction with AAV-8-GFP and AAV-9-GFP. Both vectors were able to transduce COS-1 cells effectively indicating that both vectors were functional in permissive cell types37 and data not shown.
We have previously reported the ability of anti-HIV-1 b12 minibodies to inhibit HIV-1 virus migration and infectivity using the human organotypic EpiVaginal™ tissue VEC model.37 However, a similar model for non-human primates does not currently exist. Accordingly, we adapted the procedure developed by Bobardt et al49 to examine the effects of the b12 minibodies on SHIV162p4 transfer through a monolayer of Rh PGECs (vaginal) in a transwell system. Anti-HIV-1 b12 minibodies were produced by transfecting 293 T cells with the AAV gene transfer vector pTR-b12scFvFc. SHIV162p4 virus (5 ng) with or without purified b12 scFvFc minibodies (10 ug) was then applied to the apical surface of the Rh monolayer. Following 3 hour (hr), 6 hr and overnight incubations, basal medium was collected and tested for the presence of SHIV162p4 viral particles using ELISA and infectivity assays. As shown in Figure 3, SHIV162p4 virus was effectively capable of penetrating the transwell system in the absence of an HIV-1-specific Ab as measured by p27 ELISA (Figure 3A). By contrast, in the presence of either b12 minibody or full-length b12 IgG1, SHIV162p4 transfer and infection was inhibited (Figure 3 A,B). Compared to untreated control, the inhibition of migration was 80%, 87% and 92% at 3hr, 6hr and overnight, respectively. This inhibition of migration (Figure 3A) was statistically significant at each time point (P <0.001). In addition, compared to untreated control viral infectivity was inhibited by 96% and 80% in the samples collected after 3hr and 6hr respectively in the presence of b12 minibody (p<0.0001) (Figure 3B). The inhibition by b12 minibody and b12 IgG was comparable (Pearson chi2 p=0.919 and 0.306 fat 3 hr and 6 hr, respectively). Similar results were obtained with endocervical and ectocervical monolayers in the transwell system (data not shown). These results are in agreement with published data on the ability of b12 to neutralize SHIV162p446. These findings demonstrate that b12 minibodies are comparable to full-length b12 IgG1 in their ability to inhibit SHIV162p4 transfer through vaginal epithelial cells.
Monolayers of female Rh PGECs (vaginal) were transduced by using AAV-6 vectors encoding the anti-HIV-1 b12 minibody or an irrelevant control minibody (5×1010 particles in 100 μl and at MOI of 2×105 vg/cell) to the apical surface followed by SHIV162p4 virus (5 ng in 100 μl) at 4 days post transduction. As measured by p27 ELISA, the number of SHIV162p4 viral particles that crossed monolayers in cells transduced with AAV-6 expressing control minibody was not statistically significant at 3hr and 6hrs from untransduced cells, (P < 0.17 and 0.39 respectively), the O.N. supernatant was higher for the untransduced cells (P=0.002) however at this time point most of the virus is non-infectious 49 (Figure 4). For monolayers that were transduced with AAV-6-b12 vectors, supernatants collected from the lower chambers contained significantly less SHIV162p4 viral particles compared to the no treatment controls (P< 0.001 for each time point). In addition, supernatants from AAB-6-b12 transduced cells compared to control minibody transduced cells also showed 79%, 81% and 83% inhibition of migration at 3hr, 6hr and overnight, compared to 16%, 26% and 48%, respectively, these changes were statistically significant (P< 0.005 for each time point). These data suggest that in vitro transduction of female Rh primary genital epithelial cells with AAV-6-b12 interferes with SHIV162p4 transfer through these cell monolayers.
To examine whether AAV-6 could transduce genital epithelial tissue in vivo, AAV-6-GFP 0.5 × 1012 gc/animal (the approximate estimation of the MOI is 1×105 per cell) in PBS were instilled into the vaginal vault of two female AAV-6 seronegative Rh. We chose AAV-6 seronegative animals to avoid any interaction between anti-AAV-6 antibodies and the AAV-6-GFP vectors since at this early stage of investigation we did not know what effect prior anti-AAV-6 immunity may have on the transduction efficiency and overall results. No attempt was made to remove the mucosal secretions or expose the basal epithelial layer by scarification. Vaginal and ectocervical biopsies were collected prior to transduction and at one, four, and eight weeks post transduction to evaluate GFP expression. GFP expression was observed in the cytoplasm of all layers of the cervical epithelium on day 7 in one animal, including an occasional p63 positive stem cell in the basal layer (Figure 5). No GFP positive cells were observed in the biopsy sections from 4 or 8 weeks post transduction; however, only two 1mm × 1mm blind biopsies from the vagina and two from the ectocervix were available for examination. These results indicated that AAV-6-GFP is able to transduce genital epithelial tissue in female Rh in vivo.
Next, the capacity of AAV-6-b12 vectors to induce local secretion of b12 minibodies following Rh vaginal application of AAV-6-b12 vectors (0.5 × 1012 gc/animal) was investigated in two animals. Immediately prior to application, the superficial epithelial cervical and vaginal mucosal layers were disrupted with a standard Pap smear cervical brush in order to enhance penetration of the vector to deeper cell layers and potentially prolong transgene expression. Vaginal fluids obtained from Weck-Cel wicks at varying times post transduction were recovered and b12 minibodies, which were detectable at concentrations ranging between 450 pg to 800 pg/ml (Figure 6). These results demonstrate that a single application of AAV-6-b12 vector has the capacity to transduce the lower genital tract of female Rh and to induce the secretion of b12 minibodies. Moreover, b12 minobodies were detectable over the 79 day experiment. These in vivo findings suggest that AAV-based gene transfer of BnAb b12 to the lower genital tract of female Rh could provide prolonged protection against an intravaginal SHIV162p4 challenge.
Epithelial cells of the cervical-vaginal mucosa provide the initial physical defense against HIV-1 infection. However, the protection offered by these cells is sometimes incomplete. Thus, enhancing anti-HIV-1 immunity at the mucosal cell surface by local secretion of anti-HIV-1 BnAbs to block HIV-1 entry would provide an important new intervention that could slow the spread of HIV/AIDS. To that end we constructed immortalized Rh vaginal, ecto- and endocervical cell lines and determined that AAV serotypes 2 and 6 allowed the highest level of transduction efficiency. We established Rh PGEC monolayer cultures and demonstrated in vitro inhibition of SHIV162p4 migration and infectivity using AAV-6-b12 minibody vector, a necessary step to block virus infection of susceptible immune cells present in the lamina propria of the vaginal and cervical mucosa.2
We also conducted proof-of-principle transduction studies on female Rh and demonstrated sustained detection of b12 minbodies in vaginal secretions following pre-conditioning with depoprovera and topical application of the AAV6-b12 vector. Depoprovera treatment was performed to reduce the thickness of the mucosal epithelial layers with the expectation that this would both facilitate AAV-6 gene transfer and allow in future studies efficient SHIV162p4 transmission in control treated animals 50 In two Rh, AAV6-GFP transduction and transgene expression was initially studied. Biopsy analysis of the ectocervical and vaginal mucosa demonstrated GFP expression at 7 days after topical application of the pseudovirus to the vaginal mucosa with the occasional transduction of p63+ stem cells also being seen (Figure 5E). GFP expression was not identified at time points after 7 days in the two monkeys, although only a small proportion of the ectocervix and vagina was evaluated. Indeed, the small blind biopsies limited our ability to quantitatively assess stem cell transduction frequency. This limitation may be overcome by better visibility of the cervical-vaginal mucosa using bioluminescence reporter viruses and/or multicolor fluorescence mini-endoscopic imaging.51 Indeed, the latter technique was used to follow GFP/RFP expression in mice over seven days following intravaginal transduction with papilloma GFP pseudoviruses, although the stem cell compartment was not examined.51, 52 In addition, no attempt was made in these two Rh to prepare the epithelial surface for gene transfer by removal of the protective mucosal secretions.
In two subsequently treated Rh and in order for the AAV-6-b12 vector to potentially gain easier access to the basal epithelial layers that contains p63+ stem cells, the mucosal surface was lightly scarified prior to AAV-6-b12 transduction using a standard Pap smear brush. A single application of 0.5 × 1012 gc/animal AAV-6-b12 resulted in a peak of 600-800 ng/ml b12 minibody expression in the vaginal secretions at 7 days post-transduction. In addition, the b12 minibody was detected 60-70 % of peak levels throughout the 79 day study. This result suggests that successful AAV-6 transduction had occurred at the mucosal surface, presumably including exposed epithelial stem cells (Figure 5E) however, additional studies will be required to quantify the transduction efficiency of different cell populations within the lower reproductive tract. Further refinements to the AAV vector designs29 and/or enhancements in delivery with formulations that are known to improve expression and transduction efficiency53, 54 as well as the possible use of tyrosine-modified rAAV vectors55-57 and directed evolution to increase stem cell gene transfer efficiencies57, 58 will likely improve these results. Local topical delivery of the therapy with only mild scarification equivalent to a pap smear as the preparation provides a means by which reapplication, if and when required as determined by quantitative analysis (e.g. titers by wicks), could provide better compliance than daily peri-coital microbicide applications.
We anticipate application of higher doses such as 1013 or 1014 gc/animal may yield a much higher concentration of b12 minibodies in vaginal secretions. However, the current concentration may be capable of blocking infection if translated into protection against HIV infection in humans, as most human infection via sexual encounter probably involves repeated exposures to much lower doses of virus than we used in the in vitro assays (5 ng p27 or 95 TCID50). In addition, it has been reported that lower amounts of antibody than previously considered protective may provide benefit in the context of typical human exposure to HIV-1 59. The antibody secretion titers that we observed in the present study are approaching or may have reached therapeutically relevant concentrations for the more potent human antibodies against the CD4BS or other potent neutralization epitopes27-29. While previous microbicide studies with female Rh46, 50 have demonstrated that intravaginal instillation of high concentrations of b12 IgG can afford protection against SHIV challenge, it is unknown whether the prolonged secretion of lower levels of b12 minibodies will saturate the local tissues and provide levels that are adequate to provide sustained protection against intravaginal SHIV162p4 virus challenge. In addition, in the present work, we used b12 IgG1 minibodies to establish proof-of-principle that genes encoding BnAb can be delivered to the lower genital tract of female Rh via AAV-based vectors. However, systemic protein delivery and bone marrow stem cell gene transfer approaches in humanized mice to deliver a dimeric form of b12 IgA2 showed superiority over b12 IgG1 in providing protection against intravaginal HIV-1 challenge60. Therefore, future studies should evaluate combinations of the newly reported potent BnAbs antibodies28, 61 as well as the use of IgA isotype to achieve a wider protection against HIV-1 isolates60.
Despite the positive results of using AAV vectors in a number of preclinical and clinical settings, the preexisting and/or recall immune responses to the wild-type virus from which the vector is engineered may raise some concerns about safety as well as the therapeutic efficacy. AAV-2 is the most seroprevalent in the human population, whereas seropositivity to AAV-6 is reported to be lower but it is also less studied 62-65. In our approach, we used AAV-6 vectors which were found to be resistant to the neutralizing effects of anti-AAV2 antibodies 66. Whether induction of local anti-AAV immunity will negatively impact repeated topical delivery and BnAb expression will require further evaluation. However, anti-AAV antibodies failed to block muscle transduction when the vector was directly injected intramuscularly and the development of anti-AAV antibodies did not correlate with elicitation of antibodies to the transgene 34, 67, 68. Readministration of AAV2/9 in the presence of high levels of circulating neutralizing antibodies also had minimal effect on transgene expression 40. In addition, several strategies are under investigation to mitigate immune mediated interference of AAV transgene delivery such as blockade of the TLR9-MyD88–type I IFN pathway or using empty vectors as decoys 69-71. Another safety concern is based on detection of AAV DNA in human genital tissues and in material from spontaneous abortions 72, 73. In a more recent study, the presence of AAV DNA in genital specimens was not found to be associated with clinically relevant infertility however, longitudinal studies may be required to clarify previous suggestions of an influence of AAV infection on early pregnancy problems 74.
The lack of an effective prophylactic HIV-1 vaccine has led to increased interest in anti-HIV-1 agents that can be applied topically to prevent mucosal transmission during sexual activity. A variety of compounds have been proposed as potential topical anti-HIV microbicides15, 75-78 but to date, no agent has been shown to be effective in conferring protection against HIV-1 infection with most agents failing during clinical trials. A notable exception is tenofovir gel (CAPRISA-004), which showed marginal but statistically significant protection against HIV-1 in a clinical trial.15 This trial also highlighted compliance issues with agents that required daily or timed application, and identified decreased adherence to product instructions over time by study participants. Such behavior-related issues may be pre-empted by the use of anti-HIV agents that have more sustained activity. While the benefit of using AAV-mediated anti-HIV neutralizing antibody gene transfer by systemic intravenous delivery has recently been demonstrated to provide durable protection against HIV-1 infection,29, 36 the potential safety issues of systemically transducing a wide variety of host tissues remains unknown. Our findings provide a proof-of-principle that AAV vector transduction of cervical-vaginal epithelial cells and their stem cells can lead to local and long-term secretion of a potent and broadly neutralizing anti-HIV gp120 minibody over at least several months, thus bypassing the need for daily use. The potential effects, if any, of local anti-AAV immunity on minibody expression will need to be evaluated fully. Accordingly, our data provide justification for moving this approach towards an in vivo protection study in the macaque model to determine if AAV-6-BnAb gene transfer to the lower genital tract of female Rh can lead to secretion of protective levels of neutralizing b12 antibody (Ab) and prevent infection following intravaginal SHIV162p4 challenge. Our study thus represents a novel HIV-1 microbicide strategy and potential preventative agent for HIV-1 transmission to women.
Rh macaque female genital epithelial cells were cultured in keratinocyte serum-free medium (GIBCO/BRL Life Technologies, Grand Island, NY), supplemented with bovine pituitary extract and recombinant human epidermal growth factor. The medium was further supplemented with 100 units/ml penicillin, 100 μg/ml streptomycin and CaC12 to a final calcium concentration of 0.4 mM. All other cell lines used in this study were cultured in DMEM medium supplemented with 10% FBS and 1% penicillin/streptomycin (Invitrogen, Carlsbad, CA).
The TZM-bl cell line, acquired from the National Institutes of Health AIDS Research and Reference Reagent Program (NIH-ARRRP, Germantown, MD), is a CXCR4-positive HeLa cell line that expresses CD4 and HIV-1 co-receptor CCR5; it also contains integrated reporter genes for luciferase and E. coli beta-galactosidase, under the control of an HIV long-terminal repeat sequence (tat gene) which allows for quantification of HIV infection. PA317, 293T and COS-1 cells were purchased from ATCC. All cells and cultures were maintained at 37°C in a 5% CO2 humidified incubator. The R-tropic SHIV-162p4 virus is based on molecular clones of SIVmac239 and the R5 HIV-1 primary isolate SF162 (derived from in vivo after three serial passages in Rh macaques79 was a gift from Dr. Cheng-Mayer C. (Aaron Diamond AIDS Research Center, NY).
Fresh Rh endocervical, ectocervical, and vaginal tissues were obtained as biopsies from the New England Primate Research Center, Harvard Medical School, or as explants from Tulane Primate Research Center in accordance with IACCUC regulations. Tissues were collected in cold Hanks' Balanced Salt Solution without Ca2+ and Mg 2+ and supplemented with penicillin (100 U/ml), streptomycin (100 ug/ml), and gentamicin (50 ug/ml) (GIBCO); and epithelial cells were isolated using a modified previously described protocol.48 Briefly, tissue was minced into very small pieces and then digested for 3h at 37°C in 1mg/ml of collagenase-dispase containing 1mg/ml of DNase (Sigma), with gentle stirring; the mixture was then passed through a cell strainer (250-μm), spun down (1500 rpm) for 20 min and re-suspended in DMEM with 10 % fetal calf serum (FCS). After additional centrifugation, the pellet was re-suspended in epithelial cell selection medium (Ker-sfm) inT-25 flasks; the cultures were fed every 3 days for the next 6-9 days, then sub-cultured to expand for cryopreservation and to set up cultures. Cells were passed twice prior to transduction with LXSN-16E6E7 retroviral vector packaged by the amphotropic fibroblast line PA317. Briefly, 1 ml of (LXSN-16E6E7) supernatant was used to transduce the Rhesus primary cells and then cultured in G418 selection media. Immortalized cells were then cultured in Ca2+-supplemented (0.4 mM CaCl2) keratinocyte serum-free medium. and cell stocks of the generated “primary” cell lines from vaginal, ectocervical and endocervical tissue were cryopreserved in liquid nitrogen or at −80°C after the second passage by freezing in 90% calf serum (HyClone) and 10% sulfoxide dimethyl (DMSO; Sigma).
All animal procedures including euthanasia were performed in accordance with guidelines and recommendations of The Guide for the Care and Use of Animals, the standards of the Harvard Medical School Standing Committee on Animals, and The Association for the Assessment and Accreditation of Laboratory Animal Care. Adult female Rh were confirmed serologically negative for AAV1 and AAV6 prior to inoculation, and were treated with once monthly subcutaneous Depo-Provera throughout the study period beginning 2 months prior to initial treatment. Animals were sedated using standard procedures, placed in ventral recumbency with hips elevated, followed without (AAV6-GFP) or with (AAV6-b12) pre-treatment by gentle abrasion of the vaginal and cervical mucosa with a Pap smear cervical brush (Kansas Pathology Consultants, Wichita, KS). No speculum was used to avoid loss of transduction fluid. For preparation of AAV6-b12 transduction, the cervical brush was inserted blindly and used to scarify the vagina/ectocervix. Next, Rh were intravaginally inoculated with a total volume of 0.5ml/animal of AAV-6-GFP or AAV-6-b12 (0.5 × 1012 genomic copies diluted in PBS) using a 1ml syringe that was inserted as deep as possible into the vagina. Hip elevation was maintained for 30 minutes to allow for complete absorption of the vector; no leakage was observed during or following the inoculation period. Blood samples and vaginal secretions were collected up to once a week throughout the study period, and speculum-guided cervicovaginal biopsies were obtained at weeks -1 (pre-inoculation), 1, 4, and 8.
AAV serotypes 1, 2, 5, 6, 8, and 9 expressing GFP were produced at Harvard Gene Therapy Initiative (Harvard Institute of Medicine, Boston, MA) and Penn Vector Core, University of Pennsylvania, Philadelphia, PA) whereas AAV serotypes 3 and 4 expressing GFP were obtained from the AAV core at the University of North Carolina, Chapel Hill. AAV-6 expressing b12 minibody was obtained commercially (Virapur LLC, San Diego, CA).
For AAV transduction, 5×104 Rh/V/E6E7, Rh/Ect/E6E7 and Rh/End/E6E7 immortalized cells were incubated in 24 well plates for 4 h with AAV (1, 2, 3, 4, 5, 6, 8 or 9) expressing GFP (1010 genomic copies and at MOI of 2×105 vg/cell). The medium was replaced, and the cells were examined on day 3. Expression of GFP protein was detected by flow cytometry (FACS Calibur, Becton Dickinson) and was represented as percentage of GFP positive cells, and was also assessed visually by fluorescence microscopy.
To produce the b12 minibodies, 293T cells were transfected with pTR-b12scFvFc using Lipofectamine 2000 (Invitrogen), according to the manufacturer's instructions. Sixteen hours after transfection, the media was replaced; cells were further incubated for another 48 h. The supernatant was harvested, sterile-filtered, and purified after overnight incubation at 4°C with Protein A agarose beads (GE Healthcare, Piscataway, NJ) according to the manufacturer's instructions. The b12minibody minibodies proteins were eluted with IgG elution buffer (Thermo Scientific, Waltham, MA) and the buffer was exchanged in PBS using Amicon Ultra-15 centrifugal filtration units (30 kDa molecular weight cut-off; Millipore, New Bedford, MA). Concentration of the purified b12 minibodies was measured using a human IgG ELISA kit (Bethyl Laboratories, Montgomery, TX). Ninety-six-well microtiter plates were coated overnight at 4°C with 10 ng/well of HIV-1 bal gp120 (NIH-ARRRP, Germantown, MD. Cat. # 4961) in 0.05 M carbonate-bicarbonate buffer (pH 9.6, Sigma) and blocked in PBS (1% BSA) for 1 h; serial dilutions of b12 minibodies were added to the plate for 1 h at room temperature. After washing, HRP-conjugated, affinity-purified goat anti-human IgG (Bethyl Laboratories, Montgomery, TX) was added (1:50,000) for 1 h. After extensive washing, the plate was developed by addition of TMB substrate (Kirkegaard & Perry Laboratories, Gaithersburg, MD) and detected by reading the absorbance (OD) at 450 nm.
Rh primary genital epithelial cells were seeded at a density of 105 cells/well in the upper chambers of 12-mm-diameter transwells with 3-μm-pore-size polycarbonate membranes, and cultured at 37 °C. Cells were then fed every 2 days until tight junctions formed between the cells. This was determined by measuring the changes in mechanical tension in the cell monolayer using transendothelial electrical resistance (TEER) (volt/ohm meter equipped with an electrode Millicell ERS, Millipore) (typically the tight junctions formed between days 6 and 8 after plating are about 600 ohm/m2). The cell monolayer on the filter effectively divided the well into an apical compartment and a basal compartment. To ensure the integrity of the Rh PGECs barrier, we monitored the elevated transendothelial electrical resistance of each cell monolayer which must exceed > 600 ohm/m2 and also measured the paracellular passage of Dextran-Rhodamine B (70kDa).
SHIV-162p4 viral particles that crossed the Rh macaque monolayer to the lower chambers of the transwell cultures were measured by SIV p27 antigen-capture ELISA assay (Advanced Bioscience Laboratories, Inc., Kensington, MD).
TZM-bl cells that contain a luciferase gene under the control of the HIV-1 LTR promoter were seeded in 96-well plates (4000 cells/well) and grown overnight. The medium was then removed, and cells incubated with 100 μl of media collected at different time points (up to 24 h) from the lower chambers of the Rh macaque monolayer transwell cultures. After 48 h of incubation, the cells were washed and lysed. The luciferase activity was quantified with the luciferase assay system (Promega, Cat. #E1501) and measured using the Centro LB 960 Luminometer (Berthold, Bad Wildbad, Germany).
This assay in principle is similar to an ELISA assay with the outcome measured with MSD technology, which is based on Electrochemiluminescence (ECL) detection. We used a Sulfo-Tag label that emits light upon electrochemical stimulation. Briefly, each well of a 96-well plate was coated with 5 ul of HIV-1 gp120 bal protein at 40 ug/ml, and incubated overnight at 4°C. The following day, the antigen-coated plate was incubated at 37°C for 1 h with 2% BSA blocking agent. Plates were washed with 0.05% PBS-T, and 25 μl of the diluted vaginal secretion samples were added to each well. After 1h incubation at 37°C, plates were washed with 0.05% PBS-T; and 25 μl (500ug/ml) of Sulfo-Tag-labeled goat anti-human IgG secondary antibody (Meso Scale Discovery, MD, USA Cat. # R32AJ-1) was added to each well. The plates were incubated again for 1 h at 37°C, washed and then 150 μl of MSD Read Buffer-T 4X (with surfactant) (diluted 1:4 in water) was added to each well. The plates were read using a MSD sector imager, Model no. 2400.
Immunofluorescence analysis was performed on Rh Ecto-, Endo-, and Vaginal immortalized cell lines by growing them for 3 days on 13 mm Thermanox coverslips in 24-well Falcon tissue culture plates with keratinocyte serum-free medium (ker-sfm; GIBCO) (Nunc, Naperville, IL) (Becton-Dickinson, Rutherford, NJ). Cells on coverslips were fixed with cold absolute methanol for 5 minutes and quickly rinsed with distilled water. The cell lines were then phenotyped using the specific epithelial cell markers, ck19, ck18, ck10 and secretory component (SC, polyIgA receptor) monoclonal antibodies. Cells were then examined under fluorescence microscope. Immunochemistry; Vaginal and cervical biopsies from normal Rh or Rh intra-vaginally transduced with AAV-6-GFP were fixed in 2% paraformaldehyde for 2 hours before being cryopreserved in 30% sucrose, embedded in Tissue-Tek cryo O.C.T compound (Thermo Scientific), frozen in 2-methylbutane (Fisher), and stored at −80°C. Blocks were cryosectioned at 5 microns and processed to visualize the basal epithelial layer (marker p63) with the GFP. Sections were incubated with the primary antibody for p63 (1:200, Cat # sc-8431, Santa Cruz, CA) at room temperature for 30 minutes followed by biotinylated goat anti-mouse IgG (1:200 Cat # BA9200, Vector Burlingame CA) and streptavidin 488 (1:500, Cat. # S-11223, Life Technology, Grand Island NY) for 30 minutes each. Nuclei were stained with 4',6-diamidino-2-phenylindole (DAPI) in the mounting media. Controls included isotype matched irrelevant antibodies. Tissues were then examined by fluorescence microscopy for GFP expression, using a Leica SP5 Inverted Laser Scanning Confocal Microscope (Leica Microsystems, Buffalo Grove, IL) with further image processing using ImageJ software (National Institutes of Health, Bethesda, Maryland).
All statistical evaluations were performed using Two-sample t-test. p<0.01 was considered statistically significant.
We thank Dennis Burton (The Scripps Research Institute, La Jolla, CA) for providing the scFv b12DNA plasmid, and Leonidas Stamatatos for providing the SHIV-162p4 virus. We thank clinical staff Joshua Kramer, Amber Hoggatt and Matt Beck for veterinary services and Karen Boisvert for microscopy and immunofluorescence assistance. This work was supported by NIH R21/R33 AI079767 to W.A.M, by the New England Primate Research Center Base grant P51OD011103-51 (NEPRC) and the T32 training grant T32OD011064 (SW).
The authors declare no conflict of interest.