Galton J, Ivanyi J
Eur J Immunol. 1977 Jul;7(7):457-9. doi: 10.1002/eji.1830070711.
CH strain chickens selected from the F2 progeny of a cross between CH (B10/10) and B14B (B14/14) strains carried bursa (BA) and thymus (TA)-specific alloantigens of B14B parental origin. The BA marker was present on 95% of bursal cells but only on 10% of splenic and blood B lymphocytes. The TA marker was expressed by 80% of thymus cells and weakly by 45% of splenic and 70% of blood T lymphocytes. The adopted immunological and genetic protocol offers a feasible approach towards detection of differentiation antigens in major histocompatibility complex-homozygous but 'minor' alloantigen-segregating populations.
从CH（B10/10）和B14B（B14/14）品系杂交的F2后代中选出的CH品系鸡携带了源自B14B亲本品系的法氏囊（BA）和胸腺（TA）特异性同种异体抗原。BA标记存在于95%的法氏囊细胞上，但仅存在于10%的脾脏和血液B淋巴细胞上。TA标记由80%的胸腺细胞表达，脾脏细胞的表达率为45%，血液T淋巴细胞的表达率为70%，表达较弱。所采用的免疫和遗传学方案为检测主要组织相容性复合体纯合但“次要”同种异体抗原分离群体中的分化抗原提供了一种可行的方法。
