首页   按字顺浏览 期刊浏览 卷期浏览 Immunoregulation of genetically controlled acquired responses to Leishmania donovani in...
Immunoregulation of genetically controlled acquired responses to Leishmania donovani infection in mice: the effects of parasite dose, cyclophosphamide and sublethal irradiation

 

作者: ORYSIA M. ULCZAK,   JENEFER M. BLACKWELL,  

 

期刊: Parasite Immunology  (WILEY Available online 1983)
卷期: Volume 5, issue 5  

页码: 449-463

 

ISSN:0141-9838

 

年代: 1983

 

DOI:10.1111/j.1365-3024.1983.tb00760.x

 

出版商: Blackwell Publishing Ltd

 

关键词: leishmania;acquired immunity;parasite dose;CY;irradiation

 

数据来源: WILEY

 

摘要:

SummaryOn a B10 (Lshs) genetic background, the development of acquired T cell mediated immunity to Leishmania donovani infection in mice is under H‐2 linked genetic control. Following intravenous inoculation of 107amastigotes three phenotypic patterns of recovery have been described: ‘early cure’ (H‐2r,s), ‘cure’ (H‐2b) and ‘non‐cure’ (H‐2d,q,f). In an attempt to determine the immunological basis for this H‐2 linked genetic control the effects of varying parasite dose (5 × 103to 5 × 107amastigotes) and of pre‐treatments with cyclophosphamide (50 or 200 mg/kgbody weight CY) or sublethal irradiation (100 or 550 rad) on the course of infection, and on circulating anti‐leishmanial IgG levels, were examined in strains representative of the three phenotypes: B10.D2/n (H‐2d), C57BL/10ScSn (H‐2b) and B10.RIII (H‐2r). It was found that with low parasite doses (5 × 103or 5 × 104) ‘non‐cure’ mice presented a ‘cure’ profile whilst raising the dose (5 × 107) caused some perturbation of the normal self‐curing response in ‘cure’ (but not ‘early cure’) mice. The highest dose did not, however, lead to progressive disease in the genetically non‐cure strain. For the parasite dose experiments circulating anti‐leishmanial IgG levels were higher in the early cure and cure strains than in the H‐2dnon‐cure strain. The higher doses of CY and sublethal irradiation administered prior to infection had a clear prophylactic effect on the non‐cure strain with some effect also observed in cure and early cure strains. This was thought to be due to deletion of the precursors of T suppressor (Ts) cells suppressing cell‐mediated immunity. Resolution of the liver parasite load in pre‐treated mice took place despite minimal or undetectable levels of circulating anti‐leishmanial IgG. Similarly, the earlier resolution of parasite load in pre‐treated cure and early cure mice occurred even though the antibody response was severely reduced. This suggests that the high antibody responses observed in early cure and cure strains do not normally mediate cure and may simply reflect

 

点击下载:  PDF (827KB)



返 回