Noble B, Parker D, Scheper R J, Turk J L
Immunology. 1977 Jun;32(6):885-91.
Cyclophosphamide (CY), which can enhance some forms of delayed-type hypersensitivity if given 3 days before immunization, is also a potent suppressor of most antibody mediated 4-h skin reactions to protein antigens. However many haemagglutinating antibodies, which are present in serum at the time of skin testing, are not similarly suppressed. Antibody titres in some sera recovered from CY-pretreated guinea-pigs differ little from titres in control sera. This resistance to CY suggests that long-lived precursors characterize the B-cell lines that produce many haemagglutinating antibodies, whereas the CY-sensitive precursors of skin reactive antibodies, which mediate Arthus-type reactions, are probably rapidly dividing, short-lived cells. Furthermore, the novel appearance of BGG antibodies in sera from CY-pretreated animals immunized with DNP50-BGG indicates that haemagglutinating antibody responses to some antigens are regulated by CY-sensitive mechanisms.
环磷酰胺(CY),如果在免疫前3天给予,可增强某些形式的迟发型超敏反应,它也是大多数抗体介导的对蛋白质抗原的4小时皮肤反应的强效抑制剂。然而,皮肤试验时血清中存在的许多血凝抗体并未受到类似的抑制。从经CY预处理的豚鼠中回收的一些血清中的抗体滴度与对照血清中的滴度差异不大。对CY的这种抗性表明,产生许多血凝抗体的B细胞系的特征是长寿前体,而介导阿瑟斯型反应的皮肤反应性抗体的CY敏感前体可能是快速分裂、寿命短的细胞。此外,在用DNP50-BGG免疫的经CY预处理动物的血清中BGG抗体的新出现表明,对某些抗原的血凝抗体反应受CY敏感机制调节。