Antibodies elicited against the two synthetic polypeptides, poly(Tyr,Glu)-poly(DLAla)-poly(Lys) [(T,G)-A-L] and poly(Phe,Glu)-poly(DLAla)-poly(Lys) [(Phe,G)-A-L], are crossreactive although the humoral responses to these immunogens are under different genetic controls. The fine specificity of the antibodies elicited by the two polypeptides was studied in the present work. Antisera against (Phe,G)-A-L bind both (125)I-labeled (T,G)-A-L and iodinated modified (Phe,G)-A-L. However, while the binding to (T,G)-A-L could be inhibited completely with the two antigens, the binding to (Phe,G)-A-L was inhibited completely with (Phe,G)-A-L and only partially with (T,G)-A-L. The binding of (125)I-labeled (T,G)-A-L to antisera against (T,G)-A-L was inhibted more efficiently by the homologous antigen than by (Phe,G)-A-L although both antigens completely inhibited the binding. (T,G)-A-L specific antibodies were purified on (T,G)-A-L immunoadsorbents from antisera of high and low responder mice to (T,G)-A-L immunized with (Phe,G)-A-L. (Phe,G)-A-L specific antibodies that did not bind (T,G)-A-L were isolated from the effluent of these columns. By use of anti-idiotypic antibodies of guinea pig against C3H.SW antibodies to (T,G)-A-L it was shown that (T,G)-A-L specific antibodies isolated from antisera against (Phe,G)-A-L of C3H.SW and C3H/DiSn mice possess part of the idiotypic determinants existing on antibodies of C3H.SW obtained by immunization with (T,G)-A-L. In contrast, antibodies to (Phe,G)-A-L that did not bind (T,G)-A-L did not share idiotypic determinants with C3H.SW antibody molecules against (T,G)-A-L. These results suggest that the B cell repertoire expressed by high and low responders to (T,G)-A-L after immunization with (Phe,G)-A-L is similar and represents only part of that of high responders immunized with (T,G)-A-L.
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http://dx.doi.org/10.1073/pnas.75.10.5118 | DOI Listing |
A self-reactive T cell hybridoma that secretes IL-2 in response to H-2d haplotype cells resulted from a fusion of BALB/cBy lymph node cells with the AKR thymoma BW5147. The lymph node cells used had been enriched for cells reactive to (TG)-A--L, but neither this antigen nor fetal calf serum were required for stimulation of the hybridoma designated 3DT52.5.
View Article and Find Full Text PDFJ Supramol Struct Cell Biochem
January 1982
The immune responses to several antigens were compared in the I-A mutant mouse strain B6.C-H-2bm12 and the wild-type strain C57BL/6. With a lymph node cell proliferation assay, the response to two of these antigens, beef insulin and (TG)A-L, was demonstrated to be controlled by a gene in the I-Ab region.
View Article and Find Full Text PDFThe mode of action by bystander helper T cells was investigated by priming (responder X nonresponder) (B6A)F1 T cells with poly-L-(Tyr, Glu)-poly-D,L-Ala--poly-L-Lys [(TG)-A--L] and titrating the ability of these cells to stimulate an anti-sheep red blood cell (SRBC) response of parental B cells and macrophages in the presence of (TG)-A--L. Under limiting T cell conditions, and in the presence of (TG)-A--L, (TG)-A--L-responsive T cells were able to drive anti-SRBC responses of high-responder C57BL/10.SgSn (B10) B cells and macrophages (M0), but not of low-responder (B10.
View Article and Find Full Text PDFFour different C57BL/6 mutants, each with a mutation presumably in the H-2Kb locus, were studied to determine whether the mutations had affected Ir gene function. When tested with the antigens, (TG)-A-L, ovalbumin (OA), and lactic dehydrogenase (LDHB), there was no difference in the antibody response of the mutants when compared to the parental C57BL/6 strain and there was also no difference in the response to the histocompatibility H-Y antigen. The responses to these antigens have been mapped, wholly or partially in the K-IA, IA or IB subregions and therefore the identical response of parent and mutants may provisionally exclude H-2Kb as a site of Ir gene function for the four antigens tested.
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