Three subregions of the chicken MHC (B system) encode respectively for B-F (class I), B-G, and B-L (class II) antigens. Exchanges between the B-F and B-G regions have been identified by alloimmune antisera and are maintained along with the parental haplotypes from which they arose. Together they afford unique genetic material for mapping the chicken MHC and for a variety of studies which have the potential of providing information on the roles of the subregions of the MHC in development and function of the avian immune system. Comparison of the functions of the subregions with those of H-2 in the mouse and HLA in man should provide a better understanding of the evolutionary significance of the subregions of the vertebrate MHC. To this end, a series of 12 recombinants involving B-F and B-G are immediately available for further immunogenetic study, and matings can now be made to produce recombinants of special significance. A recombinant with a large portion of the B-G region duplicated as a result of unequal crossing over will be used extensively in attempts to stimulate further unequal exchange of subregional segments. Alloimmunizations between recombinants that are similar or appear to be serologically identical with currently available reagents will be carried out in an effort to detect more subtle recombinational differences. Immunizations between selectively matched recipients and donors will be made using erythrocytes to elicit antibodies for B-F or B-G alloantigens and lymphocytes for B-L antigens. Some of the recombinants possess regional segments from parental MHC haplotypes which have been shown to influence regression of Rous sarcoma virus-induced tumors. Others involve exchange of segments between haplotypes of proven resistance and susceptibility to Marek's disease, a malignant lymphoma; data from within family segregation under challenge has shown that resistance is due to a gene or genes in or closely linked to the B-F subregion. These recombinants will be used in collaborative studies of the subregions involved in resistance to tumors and in molecular characterization of functional products of the subregions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI022957-01
Application #
3134699
Study Section
Immunobiology Study Section (IMB)
Project Start
1986-06-01
Project End
1987-11-30
Budget Start
1986-06-01
Budget End
1987-11-30
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Northern Illinois University
Department
Type
Schools of Arts and Sciences
DUNS #
City
De Kalb
State
IL
Country
United States
Zip Code
60115
Dunnington, E A; Martin, A; Briles, R W et al. (1989) Antibody responses to sheep erythrocytes for White Leghorn chickens differing in haplotypes of the major histocompatibility complex (B). Anim Genet 20:213-6
Clare, R A; Taylor Jr, R L; Briles, W E et al. (1989) Characterization of resistance and immunity to Eimeria tenella among major histocompatibility complex B-F/B-G recombinant hosts. Poult Sci 68:639-45
Kline, K; Briles, W E; Bacon, L et al. (1988) Characterization of two distinct disulfide-linked B-G molecules in the chicken. J Hered 79:249-56
Kline, K; Briles, W E; Bacon, L et al. (1988) Characterization of different B-F (MHC class I) molecules in the chicken. J Hered 79:239-48
Taylor Jr, R L; Clare, R A; Ward, P H et al. (1988) Anti-Rous sarcoma response of major histocompatibility (B) complex haplotypes B23, B24 and B30. Anim Genet 19:277-84
Briles, W E; Briles, R W (1987) Genetics and classification of major histocompatibility complex antigens of the chicken. Poult Sci 66:776-81