Voiculescu C, Stanciu L, Voiculescu M, Rogoz S, Dumitriu I
Comp Immunol Microbiol Infect Dis. 1983;6(4):291-9. doi: 10.1016/0147-9571(83)90022-x.
By using CBA/J mice as responders, the immunodepressive effect of seven antibacterial chemotherapeutic agents was tested, i.e. penicillin (pen), streptomycin (str), erythromycin (erm), kanamycin (kan), tetracycline (tet), colistin (col) and chloramphenicol (chl). Lymphocytotoxicity power, as well as the ability of each drug to influence secondary humoral (against sheep red blood cells or diphtheria anatoxin) or cell-mediated (against PPD and Coxsackie A9 virus) immunity were searched. Erm, col and chl markedly depressed humoral and cell-mediated immune responsiveness in vitro after in vivo treatment with non-cytotoxical amounts. The Th lymphocyte supplementation of B reactive spleen cell population recovered the immune capacity in col and chl in vivo-treated groups, but not in erm-treated group.
以CBA/J小鼠作为反应者,测试了七种抗菌化疗药物的免疫抑制作用,即青霉素(pen)、链霉素(str)、红霉素(erm)、卡那霉素(kan)、四环素(tet)、黏菌素(col)和氯霉素(chl)。研究了淋巴细胞毒性能力,以及每种药物影响继发性体液免疫(针对绵羊红细胞或白喉抗毒素)或细胞介导免疫(针对结核菌素纯蛋白衍生物和柯萨奇A9病毒)的能力。在用无细胞毒性剂量进行体内治疗后,红霉素、黏菌素和氯霉素在体外显著抑制体液免疫和细胞介导的免疫反应性。在体内接受黏菌素和氯霉素治疗的组中,用辅助性T淋巴细胞补充B反应性脾细胞群体恢复了免疫能力,但在接受红霉素治疗的组中则没有恢复。