Endogenous Interleukin 4 Is Required for Development of Protective CD4⁺ T Helper Type 1 Cell Responses to Candida albicans

Breeding pairs of homozygous IL-4–deficient (IL-4^−/−) and control (IL-4^+/+) BALB/c mice (23) were bred under specific, pathogen-free conditions. Mice of both sexes, 8–10 wk old, were used. Procedures involving animals and their care were conducted in conformity with national and international laws and policies.

The origin and characteristics of the C. albicans highly virulent CA-6 strain and the live vaccine strain PCA-2 used in this study have already been described in detail (4–13). For infection, cells were washed twice in saline, and diluted to the desired density to be injected intravenously via the lateral tail vein in a volume of 0.5 ml/mouse or intragastrically via an 18-gauge 4-cm-long plastic catheter, as described (24). The viability of the cells was >95% by trypan blue exclusion and quantitative cultures. Quantification of yeast cells in organs of infected mice (6–8/group) was performed by a plate-dilution method, using Sabouraud dextrose agar, and results (mean ± SEM) were expressed as CFU per organ. Resistance to reinfection was assessed by injecting mice with 10⁶ CA-6 cells intravenously, 14 d after primary infection. Mice succumbing to yeast challenge were routinely necropsied for histopathological confirmation of disseminated candidiasis. Recombinant murine IL-4 (provided by Dr. Robert Coffman, DNAX Research Institute, Palo Alto, CA) was given intraperitoneally together with the anti–IL-4 mAb 11B11 hybridoma (American Type Culture Collection, Rockville, MD; 3 μg IL-4 + 30 μg mAb, each injection) as described (12, 13). Anti–IL-4 mAb was injected intraperitoneally at the dose of 0.5 mg affinity-purified mAb/injection, as described (4, 13). Control groups were injected with saline or isotype-matched Ab (Zymed Laboratories, Inc., South San Francisco, CA). Both treatments were performed on days 6, 8, 10, and 12 after C. albicans infection. Long-lasting neutrophil depletion was obtained as described (25), by administering RB6-8C5 (anti-Ly6G) mAb intraperitoneally at the dose of 100 μg/mouse 2 d before reinfection. Endotoxin was removed from all solutions with Detoxi-gel (Pierce Chemical Co., Rockford, IL).

CD4⁺ T lymphocytes were positively selected from pools of spleen cells by means of a panning procedure using purified anti–murine CD4 mAb (GK1.5 hybridoma from American Type Culture Collection), which resulted in a >90% pure population on flow cytometric analysis (3–5). CD4⁺ cells (5 × 10⁶) were cultured in the presence of 5 × 10⁵ accessory macrophages and 5 × 10⁵ heat-inactivated yeast cells. Unfractionated splenocytes (5 × 10⁶/ml) were cultured in the presence of 10 μg/ml of Concanavalin A (Sigma Chemical Co., St. Louis, MO). Cultures of purified peritoneal neutrophils and macrophages, collected 18 or 72 h, respectively, after intraperitoneal inoculation of aged, endotoxin-free 10% thioglycollate solution (Difco, Detroit, MI), were done as described (25, 26) by incubating 5 × 10⁵ cells in the presence of IFN-γ (400 U/ml) and LPS (40 ng/ml, Sigma Chemical Co.) or 5 × 10⁴ C. albicans, PCA-2. In some experiments, cells were exposed in vitro to rIL-4 (250 U/ml) for 8 h before addition of stimuli. Cytokine measurement was performed in supernatants collected after 48 h (for lymphocytes) and 24 h (for neutrophils and macrophages).

The levels of IFN-γ, IL-2, IL-4, IL-6, and IL-10 were determined by means of cytokine-specific ELISA, using pairs of anticytokine mAbs, as described (3–13, 25, 26). The Ab pairs used were as follows, listed by capture/biotinylated detection: IFN-γ, R4-6A2/XMG1.2; IL-2, JES6-1A12/JE5H4; IL-4, BVD4-1D11/BVD6-24G2; IL-6, MP5-20F3/MP5-32c11; IL-10, JES5-2A5/SXC-1 (PharMingen, San Diego, CA). For IL-12p70 measurement, a modified Ab-capture bioassay was used, as described (7). Cytokine titers were calculated by reference to standard curves constructed with known amounts of recombinant cytokines (from PharMingen, except IL-12, from Genetics Institute, Boston, MA).

For the candidacidal assay, 5 × 10⁵ splenic macrophages (obtained by 2-h plastic adherence, >95% pure on esterase staining) or elicited peritoneal neutrophils were plated (0.1 ml/well) in 96-well flat-bottomed microtiter plates (Costar, Cambridge, MA) and incubated with 10⁵ PCA-2 cells for 4 or 1 h, respectively, as described (27). Triton X-100 (final concentration: 0.1%) was then added to the wells, and serial dilutions from each well were made in distilled water. Pour plates (four to six replicate samples) were made by spreading each sample on Sabouraud glucose agar. The number of CFU was determined after incubation at 37°C and the percentage of CFU inhibition (means ± SE) was determined as follows: percentage of colony formation inhibition = 100 − (CFU experimental group/CFU control cultures) × 100. Control cultures consisted of C. albicans cells incubated without effector cells. Nitrite concentration, a measure of nitric oxide (NO)¹ synthesis, was assayed in culture supernatants by a standard Griess reaction adapted to microplates, as described (8). The Griess reagent was prepared by mixing equal volumes of sulfanilamide (1.5% in 1 N HCl) and naphthylethylene diamine dihydrochloride (0.15% in H₂O) (Sigma Chemical Co.). A volume of 100 μl of reagent was mixed with 100 μl of supernatant and incubated for 30 min in the dark. Absorbance of the chromophore formed was measured at 540 nm in an automated microplate reader. The data represent the means ± SE of quadruplicate determinations and are expressed as μg NO₂⁻/ml.

Splenic macrophages, peritoneal neutrophils, and CD4⁺ splenocytes were subjected to RNA extraction by the guanidium thiocyanate-phenol-chloroform procedure, as described (28). In brief, 3 μg of total RNA was incubated with 0.5 μg of oligo(dT) (Pharmacia Biotech AB, Uppsala, Sweden) for 3 min at 65°C and chilled on ice for 5 min. Each sample was then incubated for 2 h at 42°C after adding 20 U RNase inhibitors (Boehringer Mannheim, Milan, Italy), 1.5 mM deoxynucleoside triphosphates, 25 U avian myeloblastosis virus reverse transcriptase (RT) (Boehringer Mannheim), and RT buffer (50 mM Tris-HCl, pH 8.3, 8 mM MgCl₂, 30 mM KCl, and 10 mM dithiothreitol, final concentrations) in a final volume of 20 μl. cDNA was diluted to a total volume of 500 μl with TE buffer (10 mM Tris-HCl, 1 mM EDTA, pH 8.0) and frozen at −20°C until use. Amplification of synthesized cDNA from each sample was carried out as described previously (29). In brief, 5 μl of cDNA was added to a reaction mixture containing 50 mM KCl, 10 mM Tris-HCl, pH 8.3, 3.0 mM MgCl₂, 0.01% gelatin, 0.2 mM deoxynucleoside triphosphates, 1 μM of each primer, and 2.5 U AmpliTaq polymerase (Perkin-Elmer Corp., Hayward, CA). Each 100-μl sample was overlaid with 75 μl mineral oil (Sigma Chemical Co.) and incubated in a DNA Thermal Cycler 480 (Perkin-Elmer Corp.) for a total of 30–35 cycles for each cytokine. For hypoxanthine-guanine phosphoribosyl transferase (HPRT) and IL-12, the primers, positive controls, cycles, and temperature were as described elsewhere (9, 10). For IL-12Rβ1, IL-12Rβ2, and IL-4R, the primers were synthesized using a 391 DNA synthesizer (PCR-MATE; Applied Biosystems, Foster City, CA). The sequences of 5′ sense primers and 3′ antisense primers for IL-12Rβ1 and IL-12Rβ2 were as follows: IL-12β1, 5′- GAA CCA CAC ACA CTG TAC CCT G, 3′- TTT AGT GGG TGG CAC GAG CC; IL-12β2, 5′- CAA GAC ATC GAC TAT GAC AGA C, 3′- CAG GTT GTG CTG TCG AGT CTC G. For IL-12Rβ1 and β2, each cycle consisted of 1 min at 94°C, 1 min at 60°C, and 1 min at 72°C. The positive controls were obtained through the courtesy of Dr. Giorgio Trinchieri (Wistar Institute, Philadelphia, PA). For IL-4R, the sequences of 5′ sense primers and 3′ antisense primers were as follows: 5′- TGT GAC CTA CAA GGA ACC CA, 3′- GCA AAA CAA CGG GAT GCA GA. For IL-4R, each cycle consisted of 1 min at 94°C, 1 min at 60°C, and 1 min at 72°C. The HPRT primers were used as a control for both reverse transcription and the PCR reaction itself, and also for comparing the amount of products from samples obtained with the same primer. The PCR fragments were analyzed by 1.5% agarose gel electrophoresis and visualized by ethidium bromide staining. PCR-assisted messenger RNA (mRNA) amplification was repeated at least twice for at least two separately prepared cDNA samples for each experiment. Data are representative of at least three different experiments.

The semiquantitative competitive PCR developed by Reiner et al. (30), was performed using the competitor construct containing sequences for multiple cytokines, the primers for HPRT and IFN-γ, and the PCR conditions described by the authors. In brief, aliquots of cDNA were assayed for levels of HPRT by placing serial dilutions from 1:1 to 1:40 of the experimental cDNA against a fixed concentration of the competitor construct and examining the ratio of competitor/wild-type band intensity after amplification with HPRT-specific primers. Adjustments were made in the amount of cDNAs needed to standardize the HPRT levels to comparable levels among all groups. Serial dilutions of these adjusted volumes of cDNA were then used to quantitate cytokine levels using a fixed concentration of competitor (3 and 1.5 pg/ml for HPRT and IFN-γ, respectively) in each reaction in the presence of cytokine-specific primers. The PCR products were separated by electrophoresis in 2% agarose gels containing ethidium bromide. The point of equivalence in intensity between the competitor (upper band) and the cDNA (lower band) indicates the relative concentration of mRNA.

Survival and organ clearance data from each group of wild-type mice were compared with those from IL-4–deficient mice using the Mann-Whitney U test; P < 0.05 was considered significant. Student's t test was used to determine statistical significance between cytokine production of the two groups. In vivo groups consisted of four to six animals. The data reported are pooled from three experiments.

IL-4^−/− and IL-4^+/+ mice were injected intravenously with different doses (10⁶, 5 × 10⁵ and 2 × 10⁵) of highly virulent CA-6, with 10⁶ cells of the live vaccine strain PCA-2, or intragastrically with 10⁸ CA-6. Mice were monitored for resistance to primary and secondary infections (Table 1) and for fungal growth in the organs (Fig. 1). The results show that, although the median survival time (MST) of mice injected with the highest inoculum of CA-6 did not differ between the two types of mice, IL-4–deficient mice were more resistant than IL-4^+/+ to the lower inocula of the yeast, as observed by the increased survival. IL-4^−/− mice were as resistant as wild-type mice to infection with PCA-2 or to intragastric infection with CA-6. However, on assaying the susceptibility of survivors to a subsequent lethal CA-6 challenge, IL-4^+/+ mice either survived or showed a remarkable resistance to reinfection, whereas IL-4–deficient mice did not.

Quantification of yeast cells recovered from infected mice revealed that the number of C. albicans cells decreased in the kidneys of IL-4^−/− mice throughout the first week of infection with either 5 × 10⁵ or 2 × 10⁵ CA-6 cells. However, at 14 d after infection, when no yeast cells were recovered in mice surviving the lowest inoculum, an extensive fungal growth was observed in the kidneys of mice succumbing to infection. In contrast, the fungal load in the kidneys of wild-type mice was always higher and increased continuously until death. In mice with gastrointestinal infection, the number of yeast cells recovered from the stomach was significantly lower in IL-4^−/− than in IL-4^+/+ mice, even though both types of mice eventually survived the infection. Resistance to CA-6 intravenous reinfection was lower in IL-4^−/− than IL-4^+/+ mice, as revealed by the high number of yeast cells recovered from the kidneys of IL-4^−/− reinfected mice. Histopathological examination of the kidneys of systemically infected IL-4–deficient mice revealed patterns of lesions similar to those observed in resistant or susceptible strains of mice infected intravenously (3– 5), with signs of extensive fungal growth and numerous foci of inflammatory reaction (mainly consisting of polymorphonuclear cells) throughout the kidney parenchyma of mice succumbing to infection and absence of pathological lesions and fungal growth in kidneys of mice resistant to infection (data not shown). Therefore, these data clearly show a two-stage control of C. albicans infection in mice. IL-4–deficient mice were highly resistant in the early stage of infection, but highly susceptible in the late stage.

To evaluate the contribution of cells of the innate immune system on the ability of IL-4–deficient mice to efficiently oppose infectivity in the early stage of infection, the antifungal effector functions of macrophages and neutrophils were assessed. Splenic macrophages and peritoneal neutrophils were obtained from IL-4^−/− and ^+/+ mice at 3 d after intravenous infection with 5 × 10⁵ CA-6 cells and assessed for candidacidal activity and production of NO. The results (Table 2) showed that the candidacidal activity of both types of cells was severely depressed in IL-4^+/+ mice upon infection, as opposed to the unimpaired activity of those from IL-4^−/− mice. Interestingly, the candidacidal activity of macrophages, and lesser that of neutrophils, appeared to be higher in uninfected IL-4^−/− mice as opposed to wild-type mice. Likewise, production of NO occurred successfully in IL-4–deficient mice, and to a lesser extent in wild-type mice. Moreover, the number of peripheral white blood cells did not differ between IL-4^−/− and IL-4^+/+ uninfected mice and increased comparably upon infection (data not shown). Therefore, these data suggest that a successful innate antifungal immune response occurs in IL-4^−/− mice upon infection.

IFN-γ is a potent activator of antifungal effector functions of phagocytic cells (31, 32) and is produced by a variety of cells, including NK and CD4⁺ Th1s (33). Therefore, we assessed the level of IFN-γ production in cultures of unfractionated or purified CD4⁺ T splenocytes obtained from mice infected with 5 × 10⁵ CA-6 cells, soon after infection. We also extended the analysis to IL-2, IL-4, and IL-10 production, as resistance and susceptibility to C. albicans is associated with preferential expansion of cells producing Th1 and Th2 cytokines, respectively (1, 2). We found that production of IFN-γ by mitogen-stimulated splenocytes was higher in IL-4^−/− than ^+/+ mice, either uninfected or at 3 d after infection, at a time when no IL-4 or minimal IL-10 were detected in the former mice compared to wild-type mice (Fig. 2). On assaying cytokine levels produced by antigen-stimulated CD4⁺ splenocytes, a similar pattern of Th1 cytokine production was observed in IL-4^−/− and ^+/+ mice, in that minimal or no IFN-γ and IL-2 were produced. As expected, IL-4 and IL-10 productions were increased in infected wild-type mice, as opposed to no (IL-4) or minimal (IL-10) detection in mutant mice (Fig. 2). Therefore, these data indicated that the early sustained production of IFN-γ in IL-4^−/− mice was derived from cells other than CD4⁺ Th1 lymphocytes.

To investigate whether CD4⁺ Th1 development may occur in IL-4–deficient mice, we measured cytokine production in culture supernatants of purified CD4⁺ splenocytes from IL-4–deficient mice infected under conditions that would otherwise result in the activation of protective CD4⁺ Th1s. For this purpose, cytokine production by splenic CD4⁺ T cells was assessed in mice reinfected with virulent CA-6, 14 d after the primary intravenous challenge with PCA-2 or after the primary intragastic challenge with CA-6. The results showed (Fig. 3) that production of IFN-γ and IL-2 were elevated, as expected, in IL-4^+/+ mice either surviving reinfection or showing increased resistance to it (Table 1). In contrast, minimal production of both cytokines was observed in IL-4 mutant mice, succumbing to reinfection. We also assessed levels of IFN-γ gene expression in CD4⁺ T cells from both types of mice by competitive PCR. IL-4^−/− and IL-4^+/+ mice were injected with PCA-2 cells and assessed for IFN-γ gene expression 3 d after reinfection with CA-6 cells. The results showed a three- to fourfold increase in the IFN-γ message in CD4⁺ cells from wild-type as compared to mutant mice (Fig. 4). Interestingly, treatment with exogenous IL-4 restored IFN-γ gene expression to a level comparable to that observed in wild-type–resistant mice.

Because IL-12 is both required and prognostic for Th1 development in mice with candidiasis (9, 10), we evaluated whether the failure of IL-4–deficient mice to default to the Th1 pathway was associated with a defective production of IL-12. We have recently shown that neutrophils, more than macrophages, are important sources of IL-12 in vivo in C. albicans infection (25, 26). Therefore, we looked for IL-12 gene expression in both neutrophils and macrophages from either type of mouse after PCA-2 infection. We found that IL-12p40 message, while present in both neutrophils and macrophages from either type of mouse soon after infection (data not shown), could not be detected in IL-4–deficient mice later in infection unless mice were treated with IL-4 (Fig. 5). The message also disappeared in IL-4^+/+ mice upon IL-4 neutralization, a finding in line with previous data (9). We also measured IL-12 responsiveness in both types of mice, by assessing levels of IL-12Rβ1 and IL-12Rβ2 expression, as it has recently been demonstrated that loss of IL-12 responsiveness, due to a selective loss of IL-12Rβ2 subunit expression, represents an early step in the commitment of T cells to the Th2 pathway (34, 35). We found that expression of the IL-12Rβ1 subunit gene was similar in either type of uninfected mice and was not modified upon C. albicans infection. For the IL-12Rβ2 subunit, expression was induced by infection and was continuously present in either type of mouse (Fig. 5). Therefore, these data suggest that IL-12 production, but not IL-12 responsiveness, was impaired in IL-4–deficient mice infected with C. albicans. To verify whether IL-12 deficiency could be responsible for the inability of IL-4–deficient mice to mount a protective CD4⁺ Th1 response, an obvious approach would have been to supply mice with exogenous IL-12. However, due to an adverse effect on neutrophils (11), administration of exogenous IL-12 to mice with candidiasis does not have a beneficial effect (9, 11). Nevertheless, the finding that in vitro exposure to IL-12 greatly increased production of IFN-γ by CD4⁺ T cells from IL-4^−/− mice cultured with Candida Ag and accessory cells (data not shown), indicated that the defective production of IL-12 may be a limiting factor in the induction of CD4⁺ Th1 responses in IL-4^−/− deficient mice.

To assess whether IL-4 would directly induce production of IL-12 in mice with candidiasis, we evaluated the effect of IL-4 priming on the ability of neutrophils and macrophages to release immunomodulating cytokines, including IL-12. Elicited peritoneal neutrophils and macrophages from IL-4–deficient mice were exposed in vitro to IL-4 before assessing cytokine levels produced in response to yeast cells. The results showed that priming with IL-4 greatly increased the ability of neutrophils, but not of macrophages, to release IL-12, with the levels of production being similar to those observed in IL-4^+/+ mice (Fig. 6,A). Interestingly, priming with IL-4 increased IL-6 production from both types of cells. The potent stimulatory effect on neutrophils appeared to be due to a direct effect of IL-4 on these cells. In fact, expression of IL-4R in response to Candida cells was induced by priming with IL-4 as opposed to what observed in macrophages, whose IL-4R expression appeared to be decreased upon IL-4 priming (Fig. 6 B). The same potentiating effect was observed by adding IL-4 and yeast cells simultaneously (data not shown). These data suggest that IL-4 may be required for an optimal production of IL-12 by neutrophils in mice with candidiasis.

We have already shown that IL-4 production late in infection is associated with the detection of protective CD4⁺ Th1s and is positively regulated by IL-12 (13). Neutralization, but not administration, of IL-4 late in the course of infection alters an already established CD4⁺ Th1 response to C. albicans (13). Here we show that treatment with IL-4 early in the course of infection greatly exacerbated the infection in both IL-4^−/− and ^+/+ mice (data not shown), as expected (12). Late treatment with IL-4 greatly increased resistance of PCA-2–infected mutant mice to reinfection, as revealed by increased survival, decreased fungal growth in the kidneys, and increased production of IFN-γ and IL-2 by CD4⁺ T cells. In contrast, IL-4 neutralization reduced resistance of wild-type mice (Table 3). To assess whether mechanisms other than regulation of IL-12 produced by neutrophils may contribute to the ability of IL-4 to sustain Th1-dependent anticandidal immunity, IL-4 was administered to IL-4^−/− and IL-4^+/+ mice depleted of neutrophils. To this purpose, groups of mice with primary infection were injected with the anti-Ly6G mAb 2 d before reinfection and treated with exogenous IL-4. Depletion of neutrophils decreased resistance to reinfection in both types of mice, as expected (25). However, exogenous IL-4 partially restored resistance of neutrophil-depleted mice, as indicated by the increased survival, decreased fungal growth, and increased production of IFN-γ and IL-2. Interestingly, the effects of IL-4 administration were similar to those observed in mice with primary infection and treated with IL-12–neutralizing Ab before reinfection (data not shown). All together these data indicate that exogenous IL-4 can increase Th1-mediated anticandidal resistance in IL-4–deficient mice, and that mechanisms other than those regulating IL-12 production by neutrophils may significantly contribute to this effect.

The results of the present study reveal a novel, previously unappreciated, role for IL-4 in vivo in mice with C. albicans infection, in which endogenous IL-4 is required for the induction of protective antifungal CD4⁺ Th1 responses. Previous studies demonstrating the beneficial (4, 5) or detrimental (12) effect of early IL-4 neutralization or administration, respectively, in mice with candidiasis led us to conclude that the occurrence of Th1 or Th2 responses positively correlated with the presence or the absence of IL-4. However, the subsequent finding that peak production of IL-4 occurred in mice with candidiasis concomitantly with the expression of protective, Th1-mediated resistance, and that depletion but not administration of IL-4 late in infection decreased resistance and production of IFN-γ and IL-12, suggested that IL-4 may have a positive effect in C. albicans infection, at least in the late stage (13). In the present study, we found that IL-4–deficient mice, while having an impaired Th2 response, did not default to the Th1 pathway, thus becoming highly susceptible in the late stage of C. albicans infection. Susceptibility to infection was not associated with signs of Th2 activation, such as production of IL-10 and high levels of circulating specific IgE (data not shown). Also, the message of IL-13 was only transiently induced in IL-4^−/− and IL-4^+/+ mice upon infection (data not shown), thus ruling out the possibility that IL-13, which signals through the IL-4Rα chain (36), may compensate for IL-4 deficiency. Therefore, IL-4 is the most important cytokine in the induction of CD4⁺ Th2 responses in candidiasis. A similar finding was observed in IL-4– deficient mice infected with a variety of pathogens, which have impaired Th2 responses but enhanced (23, 37–41) or not (14, 42) Th1 responses. We found that production of IFN-γ by CD4⁺ Th splenocytes was reduced in IL-4^−/− mice compared to wild-type mice in response to virulent C. albicans, but also in experimental conditions of infection that otherwise result in the induction of CD4⁺ Th1. Defective activation of CD4⁺ Th1 was not associated with defective IL-12 responsiveness, as the expression of IL-12Rβ2s on these cells was not different from that observed in wild-type mice mounting a CD4⁺ Th1 response. Therefore, these data indicate that the unimpaired expression of IL-12β2 on CD4⁺ cells, due to the lack of inhibitory IL-4 (34, 35), may not correlate with the functional activation of CD4⁺ Th1s in murine candidiasis.

The results obtained in the present study clearly evidence a two-stage control of infection in mice with C. albicans infection. In the early stage, an innate immune response, if unopposed, may successfully control infectivity in the absence of a supportive CD4⁺ Th1 response, as observed in IL-4–deficient mice exposed to low or moderate yeast inocula or with gastrointestinal infection. In this condition, IFN-γ derived from a non–T cell compartment, presumably NK cells (33), represents one possible activator of antifungal effector cells (31, 32). However, in the late stage of infection, IL-12 and CD4⁺ Th1s producing IFN-γ are required to cope successfully with the pathogen. Indeed, IL-4^−/− mice failed to develop protective CD4⁺ Th1 responses, as observed upon intravenous or mucosal immunization, thus becoming susceptible to infection at the late stage. Although IL-4–deficient mice appeared to be resistant to mucosal infection, the data of the present paper do not seem to suggest a possible late exacerbation of the infection, a finding compatible with the notion that IL-4 may mediate both protection (43) and pathology (44) at the mucosal level.

IL-4 appears to be required for the optimal occurrence of both innate and adaptive immune responses. Fungal elimination in IL-4^−/− BALB/c mice was not as efficient as in genetically resistant similarly infected mice (our unpublished observation), thus suggesting that IL-4 may exert a positive effect on the antifungal effector function of phagocytic cells. In this regard, IL-4 has been reported to enhance murine macrophage mannose receptor activity (45) and to stimulate phagocytosis and killing of yeast cells by macrophages (46) and neutrophils (47). Both types of cells express surface receptors for IL-4 (48, 49). We have previously reported that IL-4 inhibits candidacidal activity and NO release by macrophages (27), and in the present study we found that both activities were unimpaired in IL-4– deficient mice. It is likely that IL-4 may both positively and negatively affect the antifungal effector functions of phagocytic cells, the net result being dependent on the dose and time of infection, as observed in leishmaniasis (50).

Whatever the effect of IL-4 on the antifungal effector functions of phagocytic cells, in this study we found that IL-4 efficiently primed neutrophils for IL-12 production in response to the fungus. The effect was associated with the induction of IL-4R on these cells. That IL-4 can prime for IL-12 production has already been observed (51, 52). In human mononuclear cells (51) the positive effect of IL-4 priming on IL-12 production appeared to be due to IL-10 inhibition. Because neutrophils produce IL-12 and IL-10 in response to C. albicans (25, 26), this mechanism could be at work in our system. Interestingly, priming with IL-4 also resulted in the release of high levels of IL-6, which is known to regulate IL-4 receptors on murine myeloid progenitor cells (53). Therefore, it appears that a positive amplification loop exists between IL-6 and IL-4 at the level of neutrophil response, which may be one possible mechanism underlying the beneficial effect of IL-6 in mice with candidiasis (54).

The defective production of IL-12 may likely contribute to the impairment of CD4⁺ Th1 development in IL-4–deficient mice with C. albicans infection, as it has been shown that exposure to IL-12 restores IFN-γ production in CD4⁺ T cells from IL-4^−/− mice (22). However, the ability of IL-4 to increase IFN-γ and IL-2 production in the relative absence of neutrophils also suggests a possible direct effect of IL-4 on effector Th1s. Elegant studies by Flavell et al. have recently shown that developing Th1 lineage cells produce low levels of IL-4 as they differentiate into Th1 effectors (20, 21), thus implying that endogenous IL-4 could play an as yet not completely defined physiologic role in modulating Th1 effectors (20–22). Further studies will elucidate the important role of endogenous IL-4 in CD4⁺ Th1 differentiation and maintenance in C. albicans infection.

One interesting and still partially unresolved issue raised by our studies is where does IL-4 come from and which yeast/host factors regulate its production in mice with C. albicans infection. Evidence indicates that TCR-α/β⁺ cells, with an activated phenotype and a biased Vβ receptor expression, are the early producers of IL-4 in infected mice (55). The interaction between Candida cells and/or fungal products with cells producing IL-4 appears to occur through a superantigen-like mediated mechanism (55, 56). Whether the late peak production of IL-4 occurring in mice with candidiasis also occurs in recognition of superantigen-like molecules produced by fungal processing or fungal growth polymorphism remains an interesting possibility. Late peak production of IL-4 has also been observed in resistant mice infected with Leishmania major, and appears to be an essential component of the immune response to this parasite (57, 58).

In conclusion, this study provides several novel features of the immune response to C. albicans, including a physiologic role for IL-4 in the induction and maintenance of IL-12–dependent protective cell-mediated immunity.

The authors are grateful to Eileen Mahoney Zannetti for dedicated secretarial and editorial assistance.

This study was supported by AIDS Project 50A.0.28, Italy. The Basel Institute of Immunology has been founded and is supported by Hoffman LaRoche.