INTRODUCTION

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Adenovirus is a powerful vector for gene transfer to many tissues. Subsequent to infection, however, a strong two-phase immune response develops, impairing transgene expression: a polymorphonuclear leukocyte infiltration occurs within the first few days postinfection (p.i.) (24, 31, 60), followed by a specific immunoclearance of the infected cells. The immune effectors that come into play have been characterized in liver- and lung-directed gene transfer models. First, major histocompatibility complex (MHC) class I-restricted cytotoxic T lymphocytes (CTL) directed toward viral antigens and the transgene product target the transduced cells (11, 20, 34, 57, 61). Presentation of exogenous viral antigens by MHC class II molecules has also been implicated to induce CD4⁺ T cells of the Th1 subset that strengthen the cytotoxic response, as well as CD4⁺ T cells of the Th2 subset involved in mounting an efficient humoral response (62). The B-cell response to an adenoviral infection consists essentially of immunoglobulin G (IgG) serum antibodies, but IgA antibodies also appear within the lungs following airway administration (62). Since some of these antibodies are neutralizing, efficient adenovirus readministration is prevented (9, 14, 19). Finally, serum antibodies have been implicated in reducing the levels of the transgene product in cases for which the transgene encodes a secreted protein (31, 57).

Different strategies are being developed to counteract both arms of the host response to adenovirus infection. The first approach relies on modifying the vector backbone to limit its ability to induce a strong cellular response. E1-deleted vectors with a temperature-sensitive mutation introduced in the E2A gene were first shown to enhance transgene persistence by decreasing the cellular response (16). Vectors defective for both E1 and E4 have also been shown to lead to long-term survival of transduced hepatocytes in C57BL/6 mice immunotolerant for the transgene product (11). Similar conclusions were reached by others who showed that systemic administration of an E1/E4-defective adenovirus correlated with fewer CTLs and a prolonged transgene expression (20, 59). Adenovirus vectors with larger deletions are now being engineered that may decrease further the cellular arm of the immune response to the vector (29, 36). Although deletions of viral genes represent a potent approach for inhibiting the cellular response to the vector, it does not address the issues that stem from the humoral response directed against the capsid components.

A different means to control the host response aims at interfering directly with the many steps of this process, including inflammation. For example, a recombinant adenovirus encoding the interleukin-1 (IL-1) receptor antagonist was tested but failed to block virus-induced inflammation (40). In another study, tolerance induction following intrathymic or oral administration of adenoviral antigens was shown to be effective in abrogating the recognition phase due to the deletion or anergy of the cognate lymphocytes, translating into long-term gene delivery and efficient readministration (10, 28, 58). Administration of immunosuppressive drugs such as cyclophosphamide or cyclosporine has also been used to block the cellular and humoral arms of the immune response (50). Blocking of cell adhesion and costimulation molecules has also been tested. For example, neutralization of CD40 ligand by antibody administration has been reported to block CTL response and production of virus-specific neutralizing antibodies (63). IL-12 administration aimed at increasing the Th1/Th2 ratio has been shown to inhibit production of IgA-neutralizing antibodies and to allow successful readministration in the lung (64). By contrast, inclusion of an IL-10-like cytokine of viral origin capable of decreasing the Th1/Th2 ratio has been reported to inhibit the cellular component of the response (47). Finally, overexpression of adenovirus E3 gp19K protein has been shown to downregulate both the levels of MHC class I molecules at the cell surface and CTL induction (6, 34). Although effective, most of these strategies, however, create a profound immunosuppression. It is therefore important to assess the role of other effectors in the host response against adenoviral vectors.

Tumor necrosis factor alpha (TNF-) and lymphotoxin  (LT) are known to be important players during the development of the immune response. TNF-, which is mainly produced by activated macrophages and T cells, exists as a homotrimeric secreted molecule that binds either to TNF receptor 1 (TNFRI or p55) or TNF receptor 2 (TNFRII or p75). TNF- also exists as a transmembrane protein that binds to these same receptors for signal transduction (25). LT is another related homotrimeric secreted molecule, expressed by B and T lymphocytes, which also binds to TNFRI and TNFRII. LT also associates with lymphotoxin  (LT) to form different heterotrimeric complexes: the LT₂₁ trimer binds to both TNF- receptor types, the LT₁₂ trimer binds exclusively to a different receptor (LT receptor) (5, 8). Binding to TNFRI triggers various biological responses, such as cytolysis and inflammation. For example, TNF--induced activation of phospholipase A2 is most likely involved in cytolysis and leads to the liberation of arachidonic acid and the synthesis of prostaglandins and leukotrienes, which are very potent mediators of inflammation (32).

The importance of TNF- as a major actor in the immune response against adenovirus is supported by several independent observations. For example, TNF- has been detected at a very early stage following adenovirus administration to the lungs (24). The pivotal role of TNF- in controlling adenovirus infection is further emphasized by the existence of a set of adenovirus-encoded genes from the E3B region that counteract its function: the 14.7-kDa protein and the 10.4-kDa-14.5-kDa heterodimer act by different mechanisms to inhibit TNF--induced cytolysis and phospholipase A2 activation (30). In particular, the 10.4-kDa-14.5-kDa complex blocks the TNF--induced translocation of cytosolic phospholipase A2 to the plasma membrane, impairing the release of inflammation mediators (13). This complex also impairs FasL/Fas cytotoxicity by the release or degradation of cell surface Fas (49, 56). The E3 14.7-kDa protein interferes with TNF--induced apoptosis through its interaction with the caspase FLICE (7). The biological significance of the E3B region in controlling the immune response is further supported by assessing the in vivo behavior of specific mutant adenoviruses. For example, administration of mutants, lacking all or parts of the E3B region, into the lungs of both permissive (cotton rats) and nonpermissive (mice) animals has been correlated with an increased alveolar infiltration, compared with wild-type infection, an increase that was most likely made possible because the recruitment of inflammatory cells by TNF- byproducts was no longer inhibited (23, 51). To investigate the contribution of TNF- and its related LT in the immune response against adenovirus, we have monitored the immune parameters affected by the systemic administration of vectors in mice genetically deficient for both cytokines (1).

	MATERIALS AND METHODS

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Mice. Generation of TNF-/LT^/ mice by homologous recombination and the TNF-/LT^+/ and TNF-/LT^+/+ mice have been described (1). The mice were maintained on a mixed 129Sv × C57BL/6 genetic background in the animal facilities of the Institut Gustave Roussy (IGR) under specified pathogen-free conditions.

Adenovirus vectors. AdRSVgal and Ad1hAT encoding a nuclear -galactosidase and the human 1-antitrypsin (AT), respectively, were as described previously (22, 54). Ad-dl324 was used as an antigen in the antibody assay (55). A recombinant adenovirus AdCO1 encoding no transgene was used in the proliferation assay (26). The viral stocks were prepared on 293 cells and purified twice on CsCl gradients. Desalting was performed by using Pharmacia G50 columns (Orsay, France), and viruses were frozen in phosphate-buffered saline (PBS)-10% glycerol at 80°C. Titers were calculated as PFU on 911 cells (18).

Animals. A volume of 100 µl containing 5 × 10⁹ PFU of recombinant adenovirus diluted in PBS was injected in the retroorbital plexus of 2-month-old mice. Blood samples were collected before the virus injection and at different intervals thereafter. The sera were prepared and analyzed for serum amyloid P component (SAP), AT, and antibodies. When AdRSVgal was injected, animals were sacrificed at different days, and livers were removed for histological analysis and transgene expression assay.

Measurement of SAP. The quantity of SAP present in mouse sera was quantified by enzyme-linked immunosorbent assay (ELISA). A 96-well microtiter plate (Nunc Maxisorp, Roskilde, Denmark) was coated with 50 µl of sheep antimurine SAP antibody per well (Calbiochem, La Jolla, Calif.) diluted 1:1,000 in 50 mM NaHCO₃; after overnight incubation at 4°C, the wells were washed five times with TBSMT (Tris-buffered saline [TBS], 5% nonfat dry milk [Regilait; Nestlé, Saint-Martin-Belle-Roche, France], 0.02% Tween 20 [Sigma, Saint Quentin Fallovier, France]). Wells were blocked with TBSMT for 2 h at room temperature on a rocking platform shaker. After being washed as above, wells were incubated in TBSMT with serial dilutions of mice sera or standard murine SAP (Calbiochem). After a 2-h incubation with shaking and washing as above, wells were incubated with 50 µl of rabbit anti-murine SAP antibody (Calbiochem) diluted 1:2,000 in TBSMT. After incubation and washing as described above, wells were incubated with 50 µl of anti-rabbit antibody conjugated with alkaline phosphatase (Promega, Madison, Wis.) diluted 1:5,000 in TBSMT. After incubation and a washing as described above, SAP was detected by a 20-min incubation with developing solution (alkaline phosphatase substrate kit; Bio-Rad Laboratories, Richmond, Calif.). The A₄₀₅ was determined by using a microplate reader (Bio-Rad).

Human AT assay. The expression of AT was monitored by a sandwich ELISA as described earlier (42). Briefly, 96-well microtiter plates (Nunc) were coated with a rabbit anti-human AT antibody (Cappel; Organon Teknika, Fresnes, France), blocked with 5% milk in TBS-Tween; dilutions of sera were then added. The linked AT was revealed by using a rabbit anti-human AT Ab (Boehringer Mannheim, Meylan, France) and an alkaline phosphatase-conjugated goat anti-rabbit Ab (Promega).

Determination of adenovirus-specific antibodies. The presence of adenovirus-specific antibodies in the sera was determined by ELISA. Microplates with 96 wells (Nunc) were coated with 100 ng of inactivated adenovirus dl324 (55) and blocked with 5% milk in TBS-Tween; serial dilutions of the sera were then added. Bound antibody was detected with peroxidase-conjugated anti-mouse isotypes IgG+IgM (Jackson Immunoresearch Laboratories, West Grove, Pa.), IgG2a, IgG1, IgA, or IgM (Southern Biotechnology Associates, Birmingham, Ala.) goat antibodies. The peroxidase was revealed by incubation with the substrate o-phenylenediamine dihydrochloride (Sigma) for 30 min. The reaction was stopped by the addition of 3 N HCl, and a spectrophotometric reading was obtained at 490 nm.

Anti-adenoviral neutralizing antibody assay. 293 cells cultured in complete minimal essential medium (GIBCO-BRL) in 96-well plates (50,000 cells/well) were incubated with recombinant adenovirus (multiplicity of infection = 10) and serum dilution. Typically, a suspension of AdRSVgal (5 × 10⁵ PFU in 100 µl) was mixed with serial dilutions of serum samples decomplemented for 30 min at 56°C. This mixture was incubated with the 293 cells for 1 h at 37°C. Then, 100 µl of complete medium was added, and the cells were cultured for 19 h. Fluorometric methodology, which allows a more accurate estimation of transduction, was used. Briefly, cells were washed and incubated with 100 µl of lysis buffer (6 mM Na₂HPO₄, 10 mM KCl, 0.1 mM MgSO₄, 50 mM 2-mercaptoethanol, and 0.5% Triton X-100) containing 0.1 mg of gal substrate (4-methyl-umbelliferyl--D-galactoside; Sigma) for 1 h at 37°C. After excitation at 360 nm, the resulting fluorescence was measured at 460 nm with a Cytofluor 2300 (Millipore Corp., Bedford, Mass.). For each serum dilution, the percentage of transduction was calculated as follows: (experimental value  background value [without virus])/(positive control [100% transduction]  background value) × 100. The titer of neutralizing antibody is defined as the highest dilution which gives a percentage of transduction lower than 50%.

Determination of -galactosidase-specific antibodies. Plates (96-well; Nunc) were coated with 100 ng of -galactosidase (Sigma) and treated as described above. Serial dilutions of the sera in 5% milk in TBS-Tween were added, and bound antibody was detected with peroxidase-conjugated anti-mouse isotypes IgG+IgM (Jackson Immunoresearch Laboratories). The peroxidase activity was measured as described above.

Histochemical analysis and histopathology. After sacrifice of the animals, livers were removed at different days p.i., immediately embedded in OCT compound (Tissue-Tek; Miles Laboratories Inc., Naperville, Ill.), and snap-frozen in liquid nitrogen. For -galactosidase activity, cryosections (10 µm) were processed by postfixing in 0.37% formaldehyde-0.2% glutaraldehyde in PBS, stained with X-Gal (5-bromo-4-chloro-3-indolyl--D-galactosidase), and counterstained with hematoxylin and eosin. For inflammation analysis, liver sections were counterstained with hematoxylin and eosin and then classified as described into four groups according to the level of cellular infiltrate as follows: group 1, absent or inconspicuous infiltration; group 2, slight infiltration; group 3, moderate infiltration; and group 4, severe infiltration (11).

Immunostaining. Acetone-fixed frozen sections of liver (5 µm) were incubated with either a rat anti-CD4 antibody at a dilution of 1:3,000 or a rat anti-CD8 antibody at a dilution of 1:1,000 (PharMingen, Inc., San Diego, Calif.). For detection of macrophages, anti-Mac1 antibody was used at a dilution of 1:600 (PharMingen). After being washed, an alkaline phosphatase-conjugated rabbit anti-rat antibody (DAKO, Trappes, France) was added at a dilution of 1:50. In order to amplify the signal, an APAAP complex specific for rat (rat antibodies to calf intestinal alkaline phosphatase plus calf intestinal alkaline phosphatase) was added at a dilution of 1:25 (DAKO). Endogenous phosphatases were inhibited with levamisole (DAKO). Alkaline phosphatase activity was revealed with Fast Red substrate (DAKO), and the liver sections were counterstained with hematoxylin. As a negative control, the primary antibody was omitted in each immunostaining.

Lymphoproliferation assay. Mouse splenocytes were obtained at different times after AdRSVgal administration. Quadruplicate cultures of lymphocytes (2.5 × 10⁵ cells) were incubated in 96-well plates (Nunc) in 200 µl of RPMI supplemented with 0.6% mouse serum and 50 µM 2-mercaptoethanol with -galactosidase (0.6 µg/ml; Sigma), AdRSVgal (10 PFU/cell), or AdCO1 (10 PFU/cell, heat inactivated or not) or without antigen. Proliferation was determined on day 5 in culture after an 18-h pulse with [³H]thymidine (specific activity, 5 Ci/mmol; NEN, Le Blanc-Mesnil, France) with 1 µCi/well. Results were expressed in counts per minute (cpm) and calculated as cpm = mean cpm with antigen  mean cpm without antigen.

Cytokine release assay. Spleen cells (5 × 10⁶) from AdRSVgal-infected animals were cultured in 24-well plates (Nunc) in 2 ml of RPMI supplemented with 0.6% mouse serum and 50 µM 2-mercaptoethanol. For detection of proinflammatory cytokines, splenocytes were prepared at day 1 p.i. and cultured in the absence of any antigen, and cell-free supernatants were examined at 24 h in duplicate for the presence of IL-6 and TNF- using commercial kits (R&D Systems, Abingdon, England). For analysis of the T-helper cytokine profile, spleen cells were removed at different times and cultured either with no antigen or with heat-inactivated AdCO1 (10 PFU/cell) or recombinant -galactosidase (0.6 µg/ml). After 48 h, cell-free supernatants were collected and tested in duplicate for the presence of IL-2, gamma interferon (IFN-), and IL-4 by using commercial ELISA kits (R&D Systems).

	RESULTS

Top Abstract Introduction Materials & Methods Results Discussion References

A reduced inflammatory response was unaccompanied by a sustained expression of transgene in TNF-/LT^/ mice following recombinant adenovirus administration. In order to analyze the role played by TNF- and LT in the immune response directed against E1-deleted adenovirus, we administered 5 × 10⁹ PFU of AdRSVgal to TNF-/LT^+/+, TNF-/LT^+/, and TNF-/LT^/ mice. We first monitored the level of SAP, an acute-phase protein produced at a very early step after the inflammatory stimulus with a pic at around 24 to 36 h (53). In each experimental group, an increase in the level of SAP is observed at day 1 p.i. after adenovirus administration and is maintained until day 2 p.i. (Table 1). However, the quantity of SAP remains less in TNF-/LT^/ than in TNF-/LT^+/ and TNF-/LT^+/+ mice (80.75 µg/ml versus 114.35 and 116.15, respectively, at day 1). These data lead to a difference in SAP levels between day 1 before the virus injection and day 2 p.i. that is lower in TNF-/LT^/ mice than in the control TNF-/LT^+/ or TNF-/LT^+/+ mice (4.4 µg/ml versus 57 and 40.7 µg/ml, respectively). We also analyzed two other parameters of the inflammatory response: namely, the production of two proinflammatory cytokines TNF- and IL-6. Because these cytokines were undetectable in mice sera, supernatants of splenocytes of animals infected with adenovirus for 1 day were tested for the presence of both cytokines. A strong reduction in IL-6 levels was observed in TNF-/LT^/ mice (10.4 ± 7.4 pg/ml) versus TNF-/LT^+/ (71.9 ± 44.7 pg/ml) and TNF-/LT^+/+ (489 ± 310.2 pg/ml) mice (Fig. 1A). Interestingly, TNF-/LT^+/ mice produce less TNF- than TNF-/LT^+/+ mice (23.4 ± 0 pg/ml versus 71.5 ± 6.4 pg/ml [Fig. 1B]).

View larger version (8K): [in this window] [in a new window]   FIG. 1.   Correlation between TNF-/LT gene dosage and production of proinflammatory cytokines following adenovirus infection. The production of IL-6 (A) and TNF- (B) in the supernatant of splenocytes of TNF-/LT/, TNF-/LT+/, and TNF-/LT+/+ mice infected for 1 day was monitored by ELISA. The bar graph depicts the mean of data (n = 3) from splenocyte cultures for each mouse genotype; each triangle represents individual mouse data.

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Transgene-expressing cells are eliminated by the cellular immune response. Animals injected with AdRSVgal were analyzed for their liver cellular infiltrates (see Materials and Methods). Figure 2 depicts the increased histopathological scoring observed for all three mouse groups between days 3 and 14. There is no significant difference in the quantity of cellular infiltrates between the different groups at days 3 and 7, but the infiltrate at day 14 is clearly less important in the TNF-/LT^/ mice than in the TNF-/LT^+/+ mice. Indeed, the cellular infiltrate in TNF-/LT^/ mice never exhibits foci of inflammatory cells (grades 3 and 4 of the histopathological scoring) in liver parenchyme as was observed in TNF-/LT^+/+ mice.

View larger version (32K): [in this window] [in a new window]   FIG. 2.   Cellular infiltrate in liver of TNF-/LT-deficient mice. The relative cellular infiltrate in liver sections expressed as a histopathological score (see Materials and Methods) was evaluated at days 3, 7, and 14 p.i. Bars represent individual scores (n = 3) of TNF-/LT/ (solid bars), TNF-/LT+/ (stippled bars), or TNF-/LT+/+ (open bars) mice.

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View larger version (98K): [in this window] [in a new window]   FIG. 3.   Characterization of cellular infiltrate in the liver of adenovirus-infected mice. Immunostaining of cells positive for CD4 (A and B), CD8 (C and D), and Mac1 (E and F) was performed on liver sections of either noninfected (A, C, and E) or infected (B, D, and F) TNF-/LT/ (left) and TNF-/LT+/+ (right) mice. Magnification, ×200.

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Impaired antibody response in TNF-/LT^/ mice. We investigated the humoral response against adenovirus in all three groups of mice. The antibody level against the adenoviral capsid was analyzed in the sera at day 29 after intravenous injection of 5 × 10⁹ PFU of Ad1hAT. We observed a marked decrease in the level of total IgM and IgG antibodies in the sera of TNF-/LT^/ mice compared with the other mice (Fig. 4A). A similar defect was noticed for antibodies of the IgA isotype (Fig. 4B). Quantification of IgG subisotypes IgG1 and IgG2a indicates that the levels of both of these are very much reduced (Fig. 4C and D, respectively); it should be pointed out, however, that while some TNF-/LT^+/ and TNF-/LT^+/+ mice failed to produce significant levels of IgG2a, all of them produced IgG1 antibodies emphasizing the importance of this isotype in response to adenovirus systemic administration. On the contrary, levels of the IgM antibodies were significantly higher in the TNF-/LT^/ mice (Fig. 4E).

View larger version (18K): [in this window] [in a new window]   FIG. 4.   Impaired humoral response against adenovirus in TNF-/LT-deficient mice. Sera of TNF-/LT+/+, TNF-/LT+/, and TNF-/LT/ mice were analyzed for adenovirus-specific antibodies of different isotypes: A, IgG+IgM antibodies; B, IgA antibodies; C, IgG1 antibodies; D, IgG2a antibodies; and E, IgM antibodies. The values expressed as OD490 represent relative quantities of antibody at serum dilutions of 1:4,000 (IgG+IgM, IgG1, and IgG2a) and 1:125 (IgM and IgA). The black triangles represent antibody levels at day 29 p.i. in the serum of individual mice, and the columns represent the mean of each group.

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View larger version (12K): [in this window] [in a new window]   FIG. 5.   Impaired antibody response against the product of the transgene in TNF-/LT-deficient mice. TNF-/LT+/+, TNF-/LT+/, and TNF-/LT/ mice were injected with AdRSVgal (5 × 109 PFU). The values expressed as OD490 represent relative quantities of antibody at a serum dilution of 1:4,000 (IgG+IgM). The black triangles represent antibody levels at day 15 p.i. in the serum of individual mice, and the columns represent the mean of each group.

The absence of neutralizing antibodies allows successful virus readministration. Because of the absence of neutralizing antibodies in the TNF-/LT^/ mice, we analyzed the efficiency of a second administration. Mice were first injected with Ad1hAT (5 × 10⁹ PFU), followed by AdRSVgal (8.8 × 10⁹ PFU) 5 months later. As expected, measurement of AT levels in the serum of TNF-/LT^+/+, TNF-/LT^+/, and TNF-/LT^/ mice revealed a long-term expression (data not shown). Indeed, AT was previously reported as nonimmunogenic in the C57BL/6 background (4), and this observation was valid for our animals established on a mixed C57BL/6 × 129Sv background. Indeed, Figure 6 shows the level of -galactosidase expression in the liver at day 3 after this second administration. TNF-/LT^+/+ and TNF-/LT^+/ mice failed to express -galactosidase after readministration (Fig. 6A and B). In sharp contrast, a remarkable expression of -galactosidase was detected in TNF-/LT^/ mice (Fig. 6C). This expression in TNF-/LT^/ mice is maintained at day 8 but is no longer detectable by day 15 (data not shown). The cellular infiltrate of mononuclear cells which develops just next to the -galactosidase-positive hepatocytes in TNF-/LT^/ mice explains the loss of transgene expression. As was described for the first injection (Table 2), we observed that the titer of neutralizing antibodies at day 15 after the second injection in the TNF-/LT^/ mice still remains less than 20 (Table 3). In comparison, the antibody titer in TNF-/LT^+/+ and TNF-/LT^+/ mice rises and ranges from 1,280 to 10,240 and from 2,560 to 5,120, respectively.

View larger version (104K): [in this window] [in a new window]   FIG. 6.   Efficient readministration of recombinant adenovirus in TNF-/LT-deficient mice. Mice previously injected with Ad1hAT were secondarily injected with AdRSVgal (8.8 × 109 PFU) and sacrificed at day 3 following the second adenovirus administration. -Galactosidase expression in liver sections after X-Gal staining is shown for TNF-/LT+/+ (A), TNF-/LT+/ (B), and TNF-/LT/ (C) mice. Magnification, ×200.

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The time course of antibody response correlates with the level of TNF- and LT. We analyzed the antibody response in the sera of TNF-/LT^+/+, TNF-/LT^+/, and TNF-/LT^/ mice at different time points from the first administration of adenovirus (5 × 10⁹ PFU of Ad1hAT) till after the second injection (8.8 × 10⁹ PFU of AdRSVgal) 5 months later. At all times tested, the IgG+IgM antibody response in TNF-/LT^/ mice was very low, whereas the antibody response in TNF-/LT^+/ and TNF-/LT^+/+ mice rose to a peak at day 29 and then decreased and stabilized between days 95 and 162 (Fig. 7A1). Even after the second injection the antibody response was still lower in TNF-/LT^/ mice compared to the controls (day 177, Fig. 7A1). This is most obvious in Fig. 7A2, where a practically undetectable level of anti-adenovirus antibody in the sera of TNF-/LT^/ mice at a dilution of 1:32,000 can be seen compared to the controls. The antibody response of the IgM isotype was higher in TNF-/LT^/, mice with a maximum level evident by day 11. It decreased and remained stable until it peaked again 15 days after adenovirus readministration (Fig. 7B). This higher level of IgM antibody observed in the TNF-/LT^/ mice compared to TNF-/LT^+/ and TNF-/LT^+/+ mice is consistent with a block in the isotype switch of the humoral response. Interestingly, Fig. 7 shows that at day 11, the IgG+IgM antibody response was slightly higher in TNF-/LT^+/ mice than in TNF-/LT^+/+ mice (Fig. 7A1), which correlates well with the difference in the IgM levels observed the same day (Fig. 7B). At the other time points analyzed (days 29, 95, and 162 p.i.), the IgG+IgM antibody response against adenovirus in TNF-/LT^+/ mice was lower than in TNF-/LT^+/+ mice. Experiments carried out on larger experimental groups demonstrated that these differences between TNF-/LT^+/+ and TNF-/LT^+/ mice are statistically significant (P < 0.05) at all of the times tested, suggesting a link between antibody response against adenovirus and TNF-/LT gene dosage (data not shown).

View larger version (24K): [in this window] [in a new window]   FIG. 7.   Time course of antibody response in sera of mice deficient or not for TNF-/LT. Sera of TNF-/LT+/+ (white bars), TNF-/LT+/ (gray bars), and TNF-/LT/ (black bars) mice were obtained at different days (11, 29, 95, and 162) after the first adenovirus administration (5 × 109 PFU of Ad1hAT) and at 15 days (day 177) after the second adenovirus administration (8.8 × 109 PFU of AdRSVgal). The sera were tested for the presence of IgG+IgM antibodies (upper panel) or IgM (lower panel). The values correspond to the mean (n = 3) of relative amounts (OD490) of antibodies in sera at dilutions of 1:4,000 (A1), 1:32,000 (A2), and 1:500 (B). Accurate estimation of antibody levels at day 177 was made on sera at a dilution of 1:32,000 in order to be within the linear range of the ELISA (A2). The standard deviations are shown.

Impaired proliferative response in TNF-/LT^/ mice. We analyzed the proliferative capacity of splenocytes of AdRSVgal-infected mice at different times p.i. Data presented in Fig. 8 depicts the proliferative capacity of lymphocytes from mice of the three genotypes at day 14 p.i. with 5 × 10⁹ PFU of AdRSVgal. TNF-/LT^/ mice were profoundly impaired in their proliferative response against both viral and -galactosidase antigens, while TNF-/LT^+/ mice present an intermediate profile compared to TNF-/LT^+/+ mice. Similar results were consistently obtained with splenocytes at different times p.i. (data not shown). It should be noticed that the important difference in the proliferative capacity between mice within each group may reflect the fact that the mice used in this study are not inbred but were maintained on a mixed 129Sv × C57BL/6 background. Nevertheless, an intermediate pattern of proliferation was usually observed in TNF-/LT^+/ (Fig. 8 and data not shown), suggesting a link with TNF-/LT gene dosage. Because the T-helper response to recombinant adenovirus by intravenous delivery is known to implicate the Th1 subset in particular (61), we measured the level of IL-2 and IFN- produced by splenocytes at day 22 p.i. after in vitro restimulation with antigen. Figure 9 indicates that viral proteins (heat-inactivated adenovirus) and -galactosidase both induce the production of high levels of IL-2 (Fig. 9A) and IFN- (Fig. 9B) by splenocytes of TNF-/LT^+/+ mice (Fig. 9B) compared with unstimulated splenocytes. Upon restimulation, the levels of both cytokines were lower in TNF-/LT^+/ mice and even lower in TNF-/LT^/ mice. These results are in agreement with the defect in proliferation observed for TNF-/LT^+/ and TNF-/LT^/ mice (Fig. 8). In all three groups of mice, we detected an inconspicuous level of IL-4 (data not shown), an indicator of Th2 T cells; this is most likely because of the paucity of this population, as described by others in another model of liver gene transfer (61).

View larger version (25K): [in this window] [in a new window]   FIG. 8.   Deficient lymphoproliferative response in TNF-/LT-deficient mice. Spleen cells from mice at day 14 p.i. with 5 × 109 PFU of AdRSVgal were stimulated in vitro with AdRSVgal (10 PFU/cell [Adgal]), an adenovirus with no transgene (10 PFU/cell) that was either viable (AdCO1) or heat-inactivated (inact.), or -galactosidase (gal). The data presented on a logarithmic scale are expressed in counts per minute as indicated in Materials and Methods. The triangles represent the data (mean of quadruplicates) from the spleen of one animal, and the bars represent the mean (n = 3) of each experimental group.

View larger version (15K): [in this window] [in a new window]   FIG. 9.   Defects in Th1 cytokine production in TNF-/LT mice following adenovirus administration. Spleen cells from AdRSVgal-infected mice at day 22 p.i. were cultured in the presence of AdCO1 (Ad) or -galactosidase (gal) or in medium alone (ctrl). Supernatants were collected after 2 days and were tested in duplicate for the presence of IL-2 (A) or IFN- (B). Black triangles represent data from individual mice, and the bars represent the mean (n = 3) of each group.

	DISCUSSION

Top Abstract Introduction Materials & Methods Results Discussion References

The absence of TNF- and LT in mice results in an impaired immune response to recombinant adenovirus; this response is characterized by an attenuated acute-phase inflammation and the presence of a minor cellular infiltrate in the liver. These mice show a lack of proliferative response and an impaired humoral response against both the virus capsid and the transgene product. We report here for the first time that the absence of antiadenovirus neutralizing antibodies in this context allows an efficient secondary adenovirus-mediated gene transduction. An interesting observation lies in the correlation between TNF-/LT gene dosage and the intensity of antibody response. A detailed analysis of antibody isotypes demonstrates the lack of serum antibodies not only of the IgG but also of the IgA isotype following adenovirus administration in the absence of both TNF- and LT. That an increase in the IgM/IgG ratio is apparent in our study is consistent with the absence of isotype switching in TNF-/LT^/ mice, and this correlates with an abnormal splenic microarchitecture (33, 48). As shown in Fig. 6, these antibodies were, however, inefficient in preventing virus readministration. In another study, a disabled antibody response has been evidenced in mice after administration of an E1-deleted recombinant adenovirus expressing the E3 region from the cytomegalovirus promoter (27). In contrast to our study, a general impairment of virus-specific antibodies was documented, including IgM (27). Different immunosuppression mechanisms are therefore involved upon adenovirus injection in TNF-/LT-deficient mice versus wild-type mice injected with such an E3-overexpressing virus.

We observed a weak acute-phase inflammation process in TNF-/LT^/ and TNF-/LT^+/ mice compared to wild-type animals, with the most obvious differences at day 2 p.i. One explanation for the weak acute-phase inflammatory process we observed may be due to the fact that TNF-/LT^/ and TNF-/LT^+/ express no, or only a low level of, TNF-, a strong inducer of mouse acute-phase proteins (43). Because IL-6 is a promoter of acute-phase proteins (53), the low level of SAP observed in TNF-/LT^/ and TNF-/LT^+/ splenocytes after adenovirus infection compared to TNF-/LT^+/+ mice may also be explained by the limited ability of these mice to produce IL-6. Finally, it should be emphasized that the low levels of IL-6 in TNF-/LT^/ mice compared to TNF-/LT^+/ and to TNF-/LT^+/+ mice are in agreement with the role of TNF- as a positive regulator of IL-6 levels (52).

Binding of TNF- on TNFRI is essential for upregulation of adhesion molecules such as E-selectin and VCAM-1 and for the production of chemoattractant cytokines that are required for leukocyte organ infiltration (17, 44, 45). We thus assessed the extent of liver infiltration in our TNF-/LT^/ model and found a significant reduction compared to TNF-/LT^+/+ mice at day 16 p.i. but not at earlier time points. In contrast, an impaired intrahepatic recruitment of leukocytes has been reported as early as day 7 p.i. in TNF-/LT^/ mice (15). This difference most likely results from the absence of secondary lymphoid organs in our knockout mice due to the lack of LT receptor signaling in the absence of LT. We thus believe that leukocyte recruitment from the periportal and perivascular regions of the liver may be quicker in the absence of LT, translating at early time points p.i. into a pattern of inflammation in TNF-/LT^/ mice that is similar to that in TNF-/LT^+/+ mice. Indeed, immunostaining performed on liver sections demonstrated an increase of CD8⁺ and CD4⁺ cells in both groups of mice as early as day 7 p.i. These cells most likely illustrate an ongoing immune process by CTL and T-helper cells that might explain the absence of prolonged expression of transgene-expressing cells in TNF-/LT^/ mice. However, compared with TNF-/LT^+/+ mice, TNF-/LT^/ mice are impaired in their ability to recruit Mac1-positive cells since there is no evidence of clusters in the liver parenchyme.

After intravenous adenovirus administration in TNF-/LT^/ mice, we observed a deficient ability of T-helper lymphocytes to proliferate in response to either viral or transgene product antigen after in vitro restimulation. This deficiency is associated with a lack of production of Th1 cytokines. Such a defect in Th1 response was reported for TNF-/LT^/ mice during infection with Candida albicans (41). The absence of a T-helper proliferative response may lead to the absence of cooperation with B cells for the production of antibodies directed against a T-dependent antigen such as the adenovirus. The absence of a T-helper response may also impair the cooperation with cytotoxic T cells and may explain why TNF-/LT^/ mice exhibit an attenuated CTL response directed against vaccinia virus or lymphocytic choriomeningitis virus (17). Because such a reduction of the cytotoxic or proliferative response was not observed in TNF-^/ mice (15, 39), this defect most likely stems from the interruption of LT receptor signaling and is possibly correlated with the aberrant splenic microarchitecture.

Independent studies in different knockout models have helped to clarify the respective roles of LT and TNF- in the humoral immune response to various antigens. For example, mice lacking LT exhibit a defect in secondary lymphoid organ development and an unusual architecture of the spleen that translate into an impaired humoral immune response (3). LT^/ mice also present a defective isotype switching that has been assigned to the breakdown of signaling through the LT receptor, since normal switching occurs in both TNFRI^/ or TNFRII