Hayes C E, Hullett D A
Proc Natl Acad Sci U S A. 1982 Jun;79(11):3594-8. doi: 10.1073/pnas.79.11.3594.
T lymphocytes express a unique I-A subregion-controlled surface molecule that is not expressed on B lymphocytes. We produced antisera and monoclonal antibodies recognizing this structure. Exhaustive B cell adsorption (A.TH X B10.HTT)F antiserum, produced against activated A.TL T cells, left antibodies that bind an I-Ak specificity on some B10.A(4R) T lymphocytes (11 +/- 2%, mean +/- SEM). Similarly, exhaustive B cell adsorption of (A/J X B10.MBR)F antiserum, produced against activated B10.A(5R) cells, left antibodies specific for an I-Ab determinant on B10.A(5R)T cells (17 +/- 2%). We fused A.TL-immune (A.TH X B10.HTT)F splenocytes with NS-1 myeloma cells and identified antibody-producing hybrid cells by a fluorescent enzyme-linked immunosorbent microassay described herein. Eight monoclonal antibodies were selected; these lyse 7--26% of peripheral T cells from I-Ak strains. Thymocytes and bone marrow cells do not express the I-Ak T cells determinant. Exhaustive B cell adsorption did not remove I-Ak T cell-specific monoclonal antibodies.
T淋巴细胞表达一种独特的、受I-A亚区控制的表面分子,而B淋巴细胞不表达这种分子。我们制备了识别这种结构的抗血清和单克隆抗体。用针对活化的A.TL T细胞产生的抗血清(A.TH×B10.HTT)F进行彻底的B细胞吸附后,仍有一些抗体能与某些B10.A(4R) T淋巴细胞上的I-Ak特异性结合(11±2%,平均值±标准误)。同样,用针对活化的B10.A(5R)细胞产生的抗血清(A/J×B10.MBR)F进行彻底的B细胞吸附后,仍有针对B10.A(5R) T细胞上I-Ab决定簇的特异性抗体(17±2%)。我们将A.TL免疫的(A.TH×B10.HTT)F脾细胞与NS-1骨髓瘤细胞融合,并通过本文所述的荧光酶联免疫吸附微测定法鉴定产生抗体的杂交细胞。筛选出8种单克隆抗体;这些抗体可裂解来自I-Ak品系的7%-26%的外周T细胞。胸腺细胞和骨髓细胞不表达I-Ak T细胞决定簇。彻底的B细胞吸附并未去除I-Ak T细胞特异性单克隆抗体。