Determinant Spreading of  T Helper Cell 2 (Th2) Responses to Pancreatic Islet Autoantigens

NOD (Taconic Farms, Germantown, NY), BALB/c, and AKR mice (The Jackson Laboratory, Bar Harbor, ME) were bred under specific pathogen-free conditions. Newborn mice were treated intraperitoneally on days 1 and 3 with 200 μg of the indicated antigen in 50% IFA (GIBCO BRL, Gaithersburg, MD). Only female mice were used in these studies.

Mouse GAD (GAD65), myelin basic protein (MBP), and control Escherichia coli β-galactosidase (β-gal) were purified as previously described (1, 15). The GAD and heat shock protein peptide 277 (HSP) peptides have been reported elsewhere (1, 16, 17). Control hen egg white lysozyme (HEL) peptide HEL_11–25, immunogenic in NOD mice, was provided by Eli Sercarz (La Jolla Institute for Allergy and Immunology, La Jolla, CA). Insulin B chain and HEL were purchased from Sigma Chemical Co. (St. Louis, MO).

Splenic T cells were isolated at 4 or 12 wk of age from individual antigen-treated mice as well as unmanipulated mice, and the frequency of antigen-specific T cells secreting IFN-γ, IL-4, and IL-5 was determined using a modified ELISA spot technique (15, 18). In brief, 10⁶ splenic mononuclear cells were added per well (in triplicate) of an ELISPOT plate (Athersys, Cleveland, OH) that had been coated with cytokine capture antibodies and incubated with peptide (20 μM) or whole protein (100 μM) for 24 h for IFN-γ, or for 40 h for IL-4 and IL-5 detection. After washing, biotinylated detection antibodies were added and the plates were incubated at 4°C overnight. Bound secondary antibodies were visualized using horseradish peroxidase (HRP)–streptavidin (DAKO Corp., Carpinteria, CA) and 3-amino-9-ethylcarbazole. Antibodies R4-6A2/XMG 1.2-biotin, 11B11/BVD6-24G2-biotin, and TRFK5/TRFK4-biotin (all from PharMingen, San Diego, CA) were used for capture and detection of IFN-γ, IL-4, and IL-5, respectively.

At the time of sacrifice, sera was collected and the isotype of GAD and insulin autoantibodies were characterized using an ELISA assay as described in the legend to Fig. 1 and in reference 18. In brief, GAD (Synectics Biomedical, Stockholm) or insulin B chain at 10 μg/ml were bound to 96-well plates (Nunc), in 0.1 M NaHCO₃, pH 8.5 (GAD) or pH 9.6 (insulin B chain), at 4°C overnight. The wells were rinsed with PBS and then blocked with 3% BSA in PBS for 1 h. Mouse sera was added (0.1 ml of a 1:500 dilution) and incubated for 1 h at 37°C. After washing, bound Ig was characterized using affinity purified HRP-coupled goat anti–mouse IgG+A+M (H+L) (Pierce Chemical Co., Rockford, IL), or HRP-coupled goat anti– mouse isotype-specific antibodies for IgG₁ and IgG_2a (Southern Biotechnology Associates, Birmingham, AL) and ABTS. Sera from untreated BALB/c and AKR mice were used as negative controls.

When unmanipulated NOD mice were tested at the onset of insulitis (4 wk of age), we detected vigorous IFN-γ, but no IL-4 or IL-5 splenic T cell responses to a single determinant of GAD, GAD peptide 35, (hereafter called GADp35) consistent with a unipolar Th1 response (Table 1A). By 12 wk of age, T cell autoimmunity had spread intramolecularly to additional GAD determinants (GADp6 and GADp15) and intermolecularly to other βCAs (insulin B chain and heat shock protein, supporting earlier observations [refs 1, 2]): all of these second wave reactivities were also purely Th1 in nature (Table 1). Thus, the spontaneously developing autoimmune process is characterized by the spreading of unipolar Th1 type anti-βCA reactivity. Conceivably, the first wave of autoreactive Th1 cells, via secretion of IFN-γ and induction of IL-12, creates an environment that favors Th1 cell differentiation, generating a positive feedback loop of Th1 reactivity and amplifying proinflammatory autoimmune responses to βCAs.

We hypothesized that Th2 autoimmunity, like Th1 autoimmunity, might also spread, since the IL-4 produced by Th2 cells is itself a Th2 differentiation factor (19–22). We tested this hypothesis by inducing Th2 immunity to a single βCA and characterizing the development of T and B cell responses to unrelated βCAs.

NOD mice were neonatally treated with control antigens or βCAs in IFA, a protocol which has recently been shown to induce vigorous Th2 responses (15). NOD mice injected with the control antigens mouse MBP, HEL, or β-gal displayed vigorous IL-4 and IL-5, but no IFN-γ responses to the injected antigen, indicating the induction of unipolar Th2 responses (Table 1). Thus, NOD mice are not generally Th1 biased as has been thought, and can be manipulated to mount Th2 responses. Notably, induction of Th2 immunity to these control antigens did not affect the spontaneous development of Th1-biased anti-βCA responses (Table 1B), nor disease incidence (see below).

Neonatal injection of NOD mice with a single βCA peptide (GADp35, which contains the earliest known target determinant; reference 1), induced clear IL-4 and IL-5 responses not only to the injected peptide, but also to other GAD peptides (GADp6 and GADp15, which contain later target determinants), indicating Th2 type intramolecular spreading (Table 1A). Similarly, neonatal treatment with GADp6 led to the spreading of Th2 immunity to GADp35 and GADp15, indicating that primed Th2 responses can spread to other autoantigen determinants, independent of the order in which spontaneous autoimmune responses arise to these determinants (see Fig. 3 in reference 1). Indeed, after treatment with a GAD peptide, Th2 responses became predominant to the injected peptide, as well as to uninjected GAD peptides through intramolecular spreading. Furthermore, injection of βCAs individually (GAD, HSPp277, or insulin B chain), led to the development of Th2 autoimmunity to noninjected βCAs (intermolecular spreading, Table 1B), creating an amplificatory cascade of this antiinflammatory limb. βCA-treated NOD mice failed to respond to nontarget tissue antigens (MBP, HEL or β-gal), and in other strains of mice, primed Th2 responses to βCAs were restricted to the injected antigen (Table 1 and data not shown). NOD mouse immune responses to control nontarget tissue antigens (MBP, HEL and β-gal) were similar in magnitude to those induced by these antigens in other strains of mice (data not shown) but failed to spread to βCAs (Table 1). Thus, the spreading of Th2 responses was limited to target tissue antigens and was dependent upon a local inflammatory process.

Analysis of humoral responses showed that while unmanipulated and control antigen treated NOD mice had low levels of autoantibodies, GAD-treated animals had elevated autoantibodies to both GAD and insulin (Fig. 1), consistent with the intermolecular spreading of Th2 immunity. Similarly, neonatal treatment with insulin B chain raised the titer of GAD-specific antibodies in addition to the insulin-specific ones. The induced antibodies were of the IgG₁ subclass, characteristic of Th2 responses (19). Thus, the spreading of Th2 immunity can lead to the diversification of humoral responses.

Furthermore, the GAD peptide–treated NOD mice had significantly reduced long-term disease incidence (∼30% of GAD peptide-treated mice versus 96% of controls developed diabetes over 1 yr (P ⩽0.02); Fig. 2). The lack of complete protection by GAD treatment may be due to the diminution of Th2 responses later in life (11, 18). While the induction of Th2 responses to some nontarget tissue antigens has been associated with protection from autoimmune disease (23, 24), the control nontarget tissue antigens used in this study did not induce Th2 spreading or protection from disease.

Although we induced Th2 immunity before the onset of insulitis, βCA-treated NOD mice still developed βCA-reactive Th1 cells, suggesting that there is an inherent islet perturbation which promotes Th1 autoimmunity to βCAs. However, the Th1 responses to βCAs were markedly reduced in βCA-treated animals relative to control groups (Table 1). Despite the presence of significant Th1 responses, βCA (but not control) -treated mice displayed almost no splenic T cell proliferative responses to the injected antigen and had greatly reduced proliferative responses to other βCAs (data not shown). As the autoantibody responses in βCA-treated mice were predominantly of the Th2 type and the mice were protected from disease, it appears that Th2 immunity can be functionally dominant and a potent regulator of pathogenic Th1 activity.

In summary, we have shown in unmanipulated NOD mice that the anti-β cell response starts and spreads as a pure Th1 type autoimmunity, suggesting that a Th1 cascade underlies disease progression. Induction of Th2 autoimmunity to a single βCA resulted in the spreading of Th2 type T cell and antibody responses to other βCAs in an infectious manner. These data suggest that both Th1 and Th2 autoimmunity evolve in amplificatory cascades defined by site-specific, but not antigen-specific, positive feedback circuits, which may be generated by the cytokine milieu (24) or induced changes in accessory molecule expression (25–27). Th2 type determinant spreading introduces a novel mechanism for Th2-mediated protection, providing an explanation for the infectious nature of tolerance and why different autoantigens can be successfully used for immune therapy. Conversely, in Th2-mediated diseases, Th2 determinant spreading may contribute to the disease process, perhaps accounting for observations that in allergic conditions, individuals gradually become sensitized to an increasing number of antigens. Thus, these findings may provide a new theoretical framework for understanding disease progression in autoimmune and allergic conditions, as well as for therapeutic intervention.

This work was supported by grants from the National Institutes of Health (Bethesda, MD), the Juvenile Diabetes Foundation International, and the Riva Foundation.