Ogilvie G K, Felsburg P J, Harris C W
Veterinary Clinical Medicine, University of Illinois, Urbana 61801.
Vet Immunol Immunopathol. 1988 Mar;18(2):119-27. doi: 10.1016/0165-2427(88)90054-2.
The short-term, in vitro responses of canine peripheral blood lymphocytes to mitogenic stimulation and serum immunoglobulin concentrations were evaluated following treatment with currently recommended doses of cyclophosphamide and azathioprine. Cyclophosphamide had no significant effect on either the serum immunoglobulin concentrations or the blastogenic response of lymphocytes to mitogenic stimulation. Serum immunoglobulin concentrations remained unchanged following azathioprine treatment. The blastogenic response was significantly suppressed following one week of azathioprine therapy and returned to baseline values one week following cessation of treatment. The response to phytohemagglutinin was most suppressed, followed, in order, by the response to concanavalin A, and to pokeweed mitogen. These results suggest that the short-term use of azathioprine, but not cyclophosphamide, in clinically used dosages, does suppress selective aspects of the canine immune system, and the T cells appear to be more susceptible than B cells to the immunosuppressive effect of this drug.
在用目前推荐剂量的环磷酰胺和硫唑嘌呤治疗后,评估了犬外周血淋巴细胞对有丝分裂原刺激的短期体外反应以及血清免疫球蛋白浓度。环磷酰胺对血清免疫球蛋白浓度或淋巴细胞对有丝分裂原刺激的增殖反应均无显著影响。硫唑嘌呤治疗后血清免疫球蛋白浓度保持不变。硫唑嘌呤治疗一周后增殖反应显著受抑制,停药一周后恢复至基线值。对植物血凝素的反应受抑制程度最大,其次依次是对刀豆球蛋白A和商陆有丝分裂原的反应。这些结果表明,临床使用剂量的硫唑嘌呤而非环磷酰胺的短期使用确实会抑制犬免疫系统的某些特定方面,并且T细胞似乎比B细胞对该药物的免疫抑制作用更敏感。