The Journal of Immunology, 2008,
181,
6697
-6701
Copyright © 2008 by The American Association of Immunologists, Inc.
Cutting Edge: Helminth Infection Induces IgE in the Absence of µ- or 
-Chain Expression1
Georgia Perona-Wright*,
Katja Mohrs*,
Justin Taylor
,
Colby Zaph,
David Artis,
Edward J. Pearce and
Markus Mohrs2,*
* Trudeau Institute, Saranac Lake, NY 12983; and
Department of Pathobiology, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA 19104
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Abstract
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Infections with helminth parasites are associated with an IgE isotype switch and high serum IgE concentrations. IgE is rapidly bound by the high affinity IgE receptor (Fc
RI), thereby sensitizing FcRI-bearing basophils and mast cells for IgE-inducible effector functions such as IL-4 production. The development of Ab-secreting B cells is dependent on IgM and consequently, µMT mice, which lack surface IgM, are considered devoid of Abs. In this study we report the unexpected finding that C57BL/6 µMT mice generate robust IgE responses upon infection with three distinct helminth parasites, Heligmosomoides polygyrus, Trichuris muris, and Schistosoma mansoni. IgE is produced despite an apparent block in B cell development and licenses basophils for IgE-induced IL-4 production. Our findings reveal the existence of an evolutionarily conserved, IgM-independent pathway for the production of IgE upon infection with helminth parasites.
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Introduction
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Distant host species ranging from mouse to man mount robust IgE responses to diverse helminth parasites, indicating that the induction of IgE is an evolutionarily conserved immune mechanism. A key function of IgE is the sensitization of cells that express the high affinity IgE receptor FcRI. This licenses FcRI-bearing cells, such as basophils, to respond to IgE-mediated stimuli (1), enabling various effector functions critical to host defense including the production of IL-4 (1, 2, 3, 4, 5). Interestingly, even nonspecific IgE can elicit basophil IL-4 when engaged by soluble egg Ag of the helminth parasite Schistosoma mansoni (3). Moreover, even monomeric IgE enhances the survival and expansion of FcRI-bearing cells and increases their surface FcRI expression, creating a positive feedback loop that amplifies their sensitivity to IgE-mediated stimulation (1, 6, 7, 8, 9).
The development of B cells capable of secreting Ab is dependent on surface expression of IgM, and consequently µMT mice, which lack surface IgM and IgD, are considered devoid of Abs (10). However, µMT mice on a BALB/c background show an incomplete block in B cell development, and the presence of both serum Ig and mature B cells has been reported (11, 12). In contrast, it is generally accepted that normal B cell maturation is fully inhibited in C57BL/6 µMT animals. Nonetheless, IgA has been reported in these mice, leading to the suggestion of an evolutionary primitive system in which immature B cells switch directly to IgA production. Of note, no other isotypes, including IgE, were detected (13).
In this study we report that µMT mice on a C57BL/6 background generate robust and immunologically functional IgE responses upon infection with three distinct helminth parasites. Our data reveal an unsuspected IgM-independent pathway for the production of IgE.
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Materials and Methods
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Mice, infections, and immunization
4get (C.129-Il4tm1Lky/J) (14) mice were backcrossed to the C57BL/6 genetic background for 10 generations. All mice, including µMT (10) and JH–/– (15), were bred and housed at Trudeau Institute (Saranac Lake, NY). All animals were kept under specific pathogen-free conditions and were used at 8–12 wk of age. Mice were inoculated by gavage with 200 Heligmosomoides polygyrus (Hp)3 larvae, 200–400 embryonated Trichuris muris (Tm) eggs, or exposed percutaneously to 50 S. mansoni (Sm) cercariae as described (3, 16, 17). Two hundred Hp larvae were used for s.c. immunization. OVA/alum immunization was performed as described (3). All experimental procedures with mice were approved by the Institutional Animal Care and Use Committee of the Trudeau Institute and the University of Pennsylvania.
ELISA and ELISPOT
Serum IgE concentrations were quantified by ELISA with the paired mAbs R35-72 and R35-118 using murine IgE as a standard. The same Abs were used for ELISPOT assays; MultiScreen hemagglutinin filter plates (Millipore) were coated overnight at 4°C, blocked with FBS, and incubated with cells overnight at 37°C. IgE secretion was detected with a streptavidin-alkaline phosphatase conjugate and 5-bromo-4-chloro-3-indolyl phosphate (BCIP)/NBT substrate (Sigma-Aldrich). IL-4 in culture supernatant was quantified as described (2).
Flow cytometry and cell sorting
The following mAbs against mouse Ags were used as PE, allophycocyanin, or biotin conjugates: CCR3 (83101), CD4 (RM4-5), CD19 (6D5), CD25 (PC61), CD43 (S7), CD45R (B220; RA3-6B2), CD90.2 (Thy1.2; 53-2.1), and IgE (R35-72 and R35-118). Additional reagents included streptavidin-PE, streptavidin-allophycocyanin, and mouse anti-DNP IgE (SPE-7). Surface staining with mAb, acquisition, and analyses were performed as described (3, 14). To sort basophils, Hp-infected mice were bled on day 12 and grouped by above or below average surface IgE staining on basophils into IgEhigh and IgElow. On day 14 PBL were pooled within groups, an aliquot was stained for IgE, and GFP+CCR3–CD4– cells were sorted and cultured as described (3). B220+ and B220– cells were sorted from mesenteric LN cells from day-14 Hp-infected mice.
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Results and Discussion
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Infection-induced IgE production in the absence of IgM and IgD
Staining for FcRI-bound IgE on the surface of basophils is an immunologically relevant method for the measurement of IgE in vivo (2, 3, 8) that is more sensitive than standard serum ELISA techniques. Basophils can be identified in the blood of 4get IL-4 reporter mice as GFP+ and either CD4–SSClow or CD4–CCR3– (2, 3, 14). 4get and 4get.µMT mice, both on a C57BL/6 background, were infected with the helminth parasite Hp and 2 wk later PBL were stained with anti-IgE to detect surface-bound IgE. As expected (2, 3), strong IgE staining was observed on GFP+ cells in Hp-infected wild-type (WT) mice (Fig. 1A, left column). Surprisingly, however, IgE staining was also apparent in the vast majority of Hp-infected µMT mice (126 IgE+ of 154 Hp-infected µMT mice in 14 independent experiments). Identical results were obtained in C57BL/6 µMT mice that were not on the 4get background (see Fig. 3B). Importantly, the production of IgE in µMT mice was only observed in infected but not in naive animals (Figs. 1B and 2B).
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FIGURE 1. IgE production in the absence of IgM or IgD. A, µMT 4get (two representative mice) and C57BL/6 WT 4get mice were infected with Hp and 2 wk later PBL were analyzed by FACS for surface IgE. The presence of FcRI on basophils was demonstrated by in vitro IgE sensitization (histogram overlays). B, Individual µMT 4get mice shown before and 2 wk after infection. C, IgE staining in correlation to serum IgE concentrations, as determined by ELISA, 2 wk after infection. Dashed line indicates the limit of detection.
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FIGURE 2. IgE in µMT mice is immunologically active. A, µMT 4get and C57BL/6 WT 4get mice were infected with Hp and basophils were sorted from the indicated groups. The purified cells were stimulated in triplicates for 24 h and the production of IL-4 was determined by ELISA. B, Basophils from naive µMT 4get mice were sorted and stimulated as in A. n.d. Not detectable;  IgE, anti-IgE.
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The minority of Hp-infected µMT mice without detectable IgE retained both basophils, identified as GFP+CD4–SSClow cells, and the ability to bind IgE, as demonstrated by in vitro sensitization with IgE (Fig. 1A, middle and right columns, respectively) (2, 3). The intensity of IgE staining after in vitro sensitization was low in these animals, consistent with basal FcRI expression in the absence of IgE-induced up-regulation (8). The heterogeneity of IgE staining between individual mice correlated with serum IgE concentration (Fig. 1C) (8).
IgE in µMT mice confers immunological function
The production of IL-4 upon engagement of FcRI-bound IgE is a hallmark of basophil function (1, 2, 3, 18). To test whether the IgE in Hp-infected µMT mice confers immunological function, we isolated basophils (GFP+CD4–CCR3–) from these animals and measured the production of IL-4 in response to anti-IgE stimulation. Hp-infected µMT mice were bled before terminal PBL collection and categorized based on basophil IgE staining into an IgEhigh and an IgElow pool. Although IgE staining on the IgEhigh pool was homogeneous and comparable to that of the WT control group, the IgElow pool displayed substantial heterogeneity and a markedly reduced mean fluorescence intensity (Fig. 2, left panels). Upon stimulation with anti-IgE, all three cultures released similar amounts of IL-4 (Fig. 2A). As expected, IL-4 was undetectable in unstimulated cultures whereas the IgE-independent yet basophil-specific stimulation with IL-3 plus IL-18 also elicited IL-4 from all groups (3, 19). Consistent with the absence of IgE in naive µMT mice (Fig. 1B), basophils sorted from these animals did not produce IL-4 upon stimulation with anti-IgE but did respond to IL-3 plus IL-18 (Fig. 2B). These data demonstrate that IgE is not present in naive µMT mice, whereas even small amounts of IgE in Hp-infected µMT confer immunological function.
IgE production occurs despite a sustained block in B cell development
It has previously been shown that µMT mice on the BALB/c, but not C57BL/6, background display an incomplete block in B cell development and harbor mature B cells in secondary lymphoid organs (11, 12). Although all µMT animals used here were on a C57BL/6 background, we considered the possibility that Hp infection might overcome the B cell developmental block (10, 11, 12). CD19+B220+ B cells were not detected in the mesenteric lymph nodes (mesLN), PBL, spleen, or peritoneal cavity of Hp-infected µMT mice, whereas they were abundant in C57BL/6 WT controls (Fig. 3A and data not shown). The absence of B cells in the peritoneal cavity suggests that B-1 cells are not the source of IgE in infected µMT mice (10, 20). Consistent with a developmental arrest at the stage of pre-B cell maturation, CD19+ cells in the bone marrow of µMT mice failed to down-regulate CD43, did not induce CD25, and were present at low frequency (Fig. 3A, right panels) (10, 11, 13). As expected neither surface IgM nor IgD was detected in µMT mice even after Hp infection (data not shown) (10, 13).
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FIGURE 3. IgE-secreting cells are present despite a sustained block in B cell development. A, µMT mice and C57BL/6 WT controls were infected with Hp and analyzed 2 wk later by FACS. B, PBL of naive or 2-wk Hp-infected non-4get µMT mice and C57BL/6 WT controls as analyzed by FACS. C, PBL of B cell-deficient JH–/– mice and BALB/c WT controls analyzed by FACS 2 wk postinfection, with or without prior IgE sensitization. D, Naive or 2 wk Hp-infected mice were analyzed for basophil-bound IgE by FACS and by ELISPOT for IgE-secreting cells (ASC) in the mesLN. E, B220+ and B220– cells (see A) were sorted from the mesLN of Hp-infected µMT mice and analyzed as in D. n.d. Not detectable. F, µMT and WT mice were infected as in A and the specified populations in the mesLN were analyzed for CD11c expression.
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Given the ready detection of IgE in infected C57BL/6 µMT mice, we examined another B cell-deficient strain, JH–/– mice (15). While µMT mice lack surface expression of the µ- and 
-chains, JH–/– mice carry a deletion of the JH gene segment (10, 15). In non-4get mice, basophils can be identified by their Thy1dull phenotype in combination with IgE staining (Fig. 3B) (3, 21). Consistent with 4get µMT mice (Fig. 1), we observed robust IgE staining of Thy1dull cells in Hp-infected, but not naive, C57BL/6 µMT mice that were not on the 4get background (Fig. 3B). In contrast, no IgE was detected in Hp-infected JH–/– animals despite a clear Thy1dull basophil population able to bind IgE upon in vitro sensitization (Fig. 3C). These data demonstrate that the JH gene segment is required for infection-induced IgE production whereas the µ- and -chains are dispensable.
Because Hp-infected µMT mice produce immunologically functional IgE but no mature B cells could be identified by FACS (Fig. 3A), we used an ELISPOT assay as a functional readout to detect IgE-producing cells from the mesLN, spleen, and bone marrow of Hp-infected C57BL/6 WT, µMT, and JH–/– mice. The number of IgE-secreting cells in the mesLN of Hp-infected µMT mice was markedly increased above the background of naive controls (Fig. 3D). Substantially fewer or no IgE-secreting cells were found in µMT mice that were negative for IgE on basophils by FACS analysis. No IgE-secreting cells were detected in the spleen or bone marrow (data not shown) or in the mesLN of Hp-infected JH–/– animals (Fig. 3D). Separating mesLN cells from Hp-infected µMT mice based on the expression of B220 (Fig. 3A) identified B220– cells as the source of IgE (Fig. 3E). The B220+CD19– population in both µMT and C57BL/6 mice expressed CD11c, consistent with a plasmacytoid dendritic cell phenotype (Fig. 3F).
IgE production in µMT mice requires productive infection with diverse helminth parasites
Aluminum hydroxide (alum) is widely used as an adjuvant to elicit Th2 responses and the production of IgE (3). To test whether alum is sufficient to elicit IgE in µMT mice, we primed and boosted with OVA/alum and compared the IgE response to that induced by Hp infection. No IgE was detected on basophils isolated from OVA/alum-immunized C57BL/6 µMT mice, whereas the majority of Hp-infected µMT mice displayed high levels of IgE staining (Fig. 4A). Furthermore, IgE staining on basophils from OVA/alum-immunized mice remained low upon in vitro IgE sensitization, confirming the in vivo absence of IgE (8). These data suggest that infection with Hp larvae, and not any Th2 response, has the distinctive ability to induce IgE production in µMT mice. To determine whether the induction of IgE in µMT mice requires Hp larvae to establish productive infection in the gastrointestinal tract or whether the Th2-inducing capacity of Hp larvae alone is sufficient (22), we immunized µMT and C57BL/6 WT mice s.c. with Hp larvae. This regimen results in a potent Th2 response in the draining lymph node of both WT and µMT mice (data not shown) (22), but larval development is aborted and no intestinal infection occurs. No IgE was detected in µMT mice immunized s.c. with Hp, whereas high IgE staining was observed in WT controls (Fig. 4B). As in µMT mice challenged with OVA/alum, those immunized with Hp s.c. revealed only low levels of IgE staining upon in vitro sensitization, confirming the in vivo absence of IgE (8).
These data suggested that the production of IgE in µMT mice requires productive infection with a helminth pathogen. To explore this further, we infected µMT mice with another murine helminth parasite, Tm. In contrast to Hp, which establishes persistent infection in the small intestine, Tm infects the large intestine and is rapidly expelled (16). As shown in Fig. 4C, Tm infection also triggered IgE production in µMT mice. However, IgE was not detected in all Tm-infected animals, and IgE staining on basophils was lower than that in WT controls. These observations are consistent with the weaker Th2 response elicited by Tm than by Hp (data not shown) (16, 18). Next we infected C57BL/6 µMT mice and WT controls with Sm, a human parasite that nonetheless establishes productive and chronic infection in mice (17, 23). Although Sm resides mainly in the hepatic vasculature, eggs are continuously shed through the gastrointestinal wall. All µMT mice produced IgE upon infection with Sm, albeit at a lower level than in WT controls (Fig. 4D). These experiments demonstrate that IgE is elicited in µMT mice in response to infection with three distinct helminth parasites. Interestingly, all of these helminth parasites affect the gastrointestinal tract, and ectopic immunization of µMT mice with Hp did not result in the production of IgE. These observations are consistent with the notion that immature B cells can exit the bone marrow before terminal differentiation and receive switching signals in peripheral sites, a process that may preferentially occur in gut-associated tissue (13).
Collectively, our data demonstrate that surface expression of the Ig µ- and -chains is dispensable for the production of IgE upon infection with three distinct helminth parasites. Although the arrest in B cell development can be overcome in µMT mice on the BALB/c background, we have no evidence for a similar event in C57BL/6 µMT mice (11, 12). However, in vitro studies have shown that a direct H chain isotype switch can occur in precursor B cells in the absence of surface IgM (24). The detection of IgE in helminth-infected µMT mice likely demonstrates the relevance of this pathway in vivo. Indeed, IgE-bearing lymphocytes have been detected in a patient with X-linked agammaglobulinemia (25). Interestingly, B cell development can progress in µMT mice in the absence of the proapoptotic Fas molecule or as a consequence of forced expression of the survival factor Bcl-2 (26, 27). IL-4 was originally identified as a B cell growth and survival factor (4, 28), and thus the production of IL-4 upon helminth infection might link B cell survival with the production of IgE even in the absence of surface IgM (28). Consistent with this, Hp-infected IL-4R–/– mice produce substantially less IgE than Hp-infected µMT mice despite the presence of B cells (data not shown).
IgE enhances the expansion and survival of FcRI-bearing cells, and sensitization with IgE licenses these cells for IgE-mediated effector functions (1, 6, 7). The ability of diverse helminth parasites to elicit IgE production in the apparent absence of mature B cells suggests the engagement of an ancient, evolutionarily conserved mechanism to ensure the availability of IgE. The recent report of T cell-independent IgE production further supports the existence of such a primitive pathway (29). Importantly, based on our data, helminth-infected µMT mice can no longer be considered devoid of IgE. This has important implications for studies of helminth infections in µMT mice, which are widely used to study the role of IgE in type 2 immune responses.
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Acknowledgments
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We thank Frances Lund and Susan Swain for reagents, Brandon Sells for cell sorting, and Cris Kamperschroer for technical advice.
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Disclosures
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The authors have no financial conflict of interest.
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Footnotes
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The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
1 This work was supported by funds from Trudeau Institute and the National Institutes of Health Grants AI61570 (to D.A.), AI074878 (to D.A.), AI32573 (to E.J.P.), AI072296 (to M.M.), and AI076479 (to M.M.). 
2 Address correspondence and reprint requests to Dr. Markus Mohrs, Trudeau Institute, 154 Algonquin Avenue, Saranac Lake, NY 12983. E-mail address: mmohrs{at}trudeauinstitute.org
3 Abbreviations used in this paper: Hp, Heligmosomoides polygyrus; mesLN, mesenteric lymph node; Sm, Schistosoma mansoni; Tm, Trichuris muris; WT, wild type.
Received for publication April 16, 2008.
Accepted for publication September 19, 2008.
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Abstract
Introduction
