Abstract
We previously reported that BCG-induced anergy in mice (evaluated by delayed hypersensitivity to sheep erythrocytes) is unigenic and influenced by genes linked to the immunoglobulin heavy chain allotype (Igh). Using congenic mice (either H-2k or H-2b), we could not detect H-2-linked control of anergy. The current study re-examines this issue by using both BXD (H-2b or H-2d) and BXH (H-2b or H-2k) recombinant inbred (RI) mice as well as H-2 recombinant mice of different haplotypes. BXD RI (H-2b) mice were more anergic than BXD RI (H-2d) animals. Also, BXD RI (Ighb animals were more anergic than BXD RI (Ighc) mice. By evaluating combinations of H-2 haplotypes and Igh allotypes, we found the most anergic animals to be H-2b, Ighb. BCG-induced anergy then appears to be influenced by genes linked to both the H-2 and Igh complexes. BCG-induced anergy developed in H-2 recombinant mice (C57BL/10 background) that were either H-2b or H-2k, but not in H-2d animals. Experiments in the B10.A mouse suggested that genes within the H-2K through H-2I were influential. A more definitive map is presented of Igh-linked genes influencing anergy, suggesting that these genes are approximately 23 recombination units on the centromeric side of Igh-1 between Igh-Src and Lyb-7.
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Selected References
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- Allen E. M., Moore V. L., Stevens J. O. Strain variation in BCG-induced chronic pulmonary inflammation in mice. I. Basic model and possible genetic control by non-H-2 genes. J Immunol. 1977 Jul;119(1):343–347. [PubMed] [Google Scholar]
- Allen E. M., Moore V. L. Suppression of phytohemagglutinin and lipopolysaccharide responses in mouse spleen cells by Bacillus Calmette-Guerin. J Reticuloendothel Soc. 1979 Oct;26(4):349–356. [PubMed] [Google Scholar]
- Allen E. M., Sternick J. L., Schrier D. J., Moore V. L. BCG-induced chronic pulmonary inflammation and splenomegaly in mice: suppression of PHA-induced proliferation, delayed hypersensitivity to sheep erythrocytes, and chronic pulmonary inflammation by soluble factors from adherent spleen cells. Cell Immunol. 1981 Feb;58(1):61–71. doi: 10.1016/0008-8749(81)90149-0. [DOI] [PubMed] [Google Scholar]
- Asherson G. L., Stone S. H. Desensitization in vitro--the specific inhibition, by antigen, of the passive transfer of delayed hypersensitivity by peritoneal exudate cells. Immunology. 1967 Nov;13(5):469–475. [PMC free article] [PubMed] [Google Scholar]
- Aune T. M., Pierce C. W. Identification and initial characterization of a nonspecific suppressor factor (macrophage-SF) produced by soluble immune response suppressor (SIRS)-treated macrophages. J Immunol. 1981 Nov;127(5):1828–1833. [PubMed] [Google Scholar]
- Aune T. M., Pierce C. W. Mechanism of action of macrophage-derived suppressor factor produced by soluble immune response suppressor-treated macrophages. J Immunol. 1981 Jul;127(1):368–372. [PubMed] [Google Scholar]
- Berek C., Taylor B. A., Eichmann K. Genetics of the idotype of BALB/c myeloma S117: multiple chromosomal loci for Vh genes encoding specificity for group A streptococcal carbohydrate. J Exp Med. 1976 Nov 2;144(5):1164–1174. doi: 10.1084/jem.144.5.1164. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bullock W. E. Anergy and infection. Adv Intern Med. 1976;21:149–173. [PubMed] [Google Scholar]
- Bullock W. E., Carlson E. M., Gershon R. K. The evolution of immunosuppressive cell populations in experimental mycobacterial infection. J Immunol. 1978 May;120(5):1709–1716. [PubMed] [Google Scholar]
- Dwyer J. M., Bullock W. E., Fields J. P. Disturbance of the blood T:B lymphocyte ratio in lepromatous leprosy. Clinical and immunologic correlations. N Engl J Med. 1973 May 17;288(20):1036–1039. doi: 10.1056/NEJM197305172882002. [DOI] [PubMed] [Google Scholar]
- Dwyer J. M., Kantor F. S. In vivo suppression of delayed hypersensitivity: prolongation of desensitization in guinea pigs. J Exp Med. 1975 Sep 1;142(3):588–599. doi: 10.1084/jem.142.3.588. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Green W. F., Colley D. G. Modulation of Schistosoma mansoni egg-induced granuloma formation: I-J restriction of T cell-mediated suppression in a chronic parasitic infection. Proc Natl Acad Sci U S A. 1981 Feb;78(2):1152–1156. doi: 10.1073/pnas.78.2.1152. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hahn H., Kaufmann S. H., Miller T. E., Mackaness G. B. Peritoneal exudate T lymphocytes with specificity to sheep red blood cells. I. Production and characterization as to function and phenotype. Immunology. 1979 Apr;36(4):691–698. [PMC free article] [PubMed] [Google Scholar]
- Ju S. T., Dorf M. E. Idiotypic analysis of anti-GAT antibodies. IX. Genetic mapping of the Gte idiotypic marker within the Igh-V locus. J Immunol. 1981 Jan;126(1):183–186. [PubMed] [Google Scholar]
- Kipps T. J., Benacerraf B., Dorf M. E. Presence of common idiotypes on antibodies induced by glutamic acid-lysine-containing terpolymers in responder and nonresponder mice with the Ig-1b heavy chain allotype. Eur J Immunol. 1977 Dec;7(12):865–871. doi: 10.1002/eji.1830071209. [DOI] [PubMed] [Google Scholar]
- Lagrange P. H., Mackaness G. B., Miller T. E. Influence of dose and route of antigen injection on the immunological induction of T cells. J Exp Med. 1974 Mar 1;139(3):528–542. doi: 10.1084/jem.139.3.528. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mangi R. J., Dwyer J. M., Gee B., Kantor F. S. The immunological competence of subjects with sarcoidosis. Clin Exp Immunol. 1974 Dec;18(4):505–517. [PMC free article] [PubMed] [Google Scholar]
- McCarthy M. M., Dutton R. W. The humoral response of mouse spleen cells to two types of sheep erythrocytes. III. A new VH region marker. J Immunol. 1975 Nov;115(5):1327–1329. [PubMed] [Google Scholar]
- Papermaster V., Yoshida T., Cohen S. Desensitization. II. Passive Transfer of the desensitized state by serum from desensitized animals. Cell Immunol. 1978 Feb;35(2):378–391. doi: 10.1016/0008-8749(78)90157-0. [DOI] [PubMed] [Google Scholar]
- Pelley R. P., Warren K. S. Immunoregulation in chronic infectious disease: schistosomiasis as a model. J Invest Dermatol. 1978 Jul;71(1):49–55. doi: 10.1111/1523-1747.ep12543940. [DOI] [PubMed] [Google Scholar]
- Pierce C. W. Macrophages: modulators of immunity. Parke-Davis Award Lecture. Am J Pathol. 1980 Jan;98(1):10–28. [PMC free article] [PubMed] [Google Scholar]
- Ptak W., Zembala M., Gershon R. K. Intermediary role of macrophages in the passage of suppressor signals between T-cell subsets. J Exp Med. 1978 Aug 1;148(2):424–434. doi: 10.1084/jem.148.2.424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schrier D. J., Allen E. M., Moore V. L. BCG-induced macrophage suppression in mice: suppression of specific and nonspecific antibody-medicated and cellular immunologic responses. Cell Immunol. 1980 Dec;56(2):347–356. doi: 10.1016/0008-8749(80)90110-0. [DOI] [PubMed] [Google Scholar]
- Schrier D. J., Sternick J. L., Allen E. M., Moore V. L. Genetic basis of BCG-induced suppression of delayed hypersensitivity. Nature. 1981 Jan 29;289(5796):405–407. doi: 10.1038/289405a0. [DOI] [PubMed] [Google Scholar]
- Schrier D. J., Sternick J. L., Allen E. M., Moore V. L. Immunogenetics of BCG-induced anergy in mice: control by genes linked to the Igh complex. J Immunol. 1982 Mar;128(3):1466–1469. [PubMed] [Google Scholar]
- Sonozaki H., Papermaster V., Yoshida T., Cohen S. Desensitization: effects on cutaneous and peritoneal manifestations of delayed hypersensitivity in relation to lymphokine production. J Immunol. 1975 Dec;115(6):1657–1661. [PubMed] [Google Scholar]
- Subbarao B., Ahmed A., Paul W. E., Scher I., Lieberman R., Mosier D. E. Lyb-7, a new B cell alloantigen controlled by genes linked to the IgCH locus. J Immunol. 1979 Jun;122(6):2279–2285. [PubMed] [Google Scholar]
- Tadakuma T., Pierce C. W. Mode of action of a soluble immune response suppressor (SIRS) produced by concanavalin a-activated spleen cells. J Immunol. 1978 Feb;120(2):481–486. [PubMed] [Google Scholar]
- Taylor B. A., Bailey D. W., Cherry M., Riblet R., Weigert M. Genes for immunoglobulin heavy chain and serum prealbumin protein are linked in mouse. Nature. 1975 Aug 21;256(5519):644–646. doi: 10.1038/256644a0. [DOI] [PubMed] [Google Scholar]
- Thestrup-Pedersen K., Dwyer J. M., Askenase P. W. Studies on the role of the thymus and T cells in the in vivo suppression of delayed hypersensitivity (desensitization): radiosensitivity of the mechanism inducing nonspecific anergy. J Immunol. 1977 May;118(5):1665–1671. [PubMed] [Google Scholar]
- UHR J. W., PAPPENHEIMER A. M., Jr Delayed hypersensitivity. III. Specific desensitization of guinea pigs sensitized to protein antigens. J Exp Med. 1958 Dec 1;108(6):891–904. doi: 10.1084/jem.108.6.891. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Uno H., Sasazuki T., Tamai H., Matsumoto H. Two major genes, linked to HLA and Gm, control susceptibility to Graves' disease. Nature. 1981 Aug 20;292(5825):768–770. doi: 10.1038/292768a0. [DOI] [PubMed] [Google Scholar]
- Wagshal A. B., Jegasothy B. V., Waksman B. H. Regulatory substances produced by lymphocytes. VI. Cell cycle specificity of inhibitor of DNA synthesis action in L cells. J Exp Med. 1978 Jan 1;147(1):171–181. doi: 10.1084/jem.147.1.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
