TY - JOUR KW - Animals KW - Antigens, Bacterial KW - Cercocebus atys KW - Disease Models, Animal KW - Enzyme-Linked Immunosorbent Assay KW - Glycolipids KW - Immunoglobulin G KW - Immunoglobulin M KW - leprosy KW - Lipopolysaccharides KW - Longitudinal studies KW - Mycobacterium leprae AU - Gormus B J AU - Xu K AU - Cho S N AU - Baskin G B AU - Bohm R P AU - Martin L N AU - Blanchard J L AU - Mack P A AU - Ratterree M S AU - Meyers W M AB -
In this study, 11 SMM were grouped and inoculated with differing doses of SMM-origin Mycobacterium leprae (ML) between 4.5 x 10(8) and 1 x 10(9) by either combined IV/IC routes or by IV or IC route alone. The combined route was the most effective in eliciting progressive, disseminated LL leprosy. In all, 6 of 7 SMM inoculated by the combined routes developed leprosy requiring treatment at some point. Only 1 of 4 inoculated by a single route developed persisting leprosy requiring chemotherapy. Either no disease or spontaneous regression of initial disease occurred in the other 3 animals inoculated by a single route. Doses in excess of 1 x 10(9) ML were more effective than lesser doses. An association was observed between the development of IgG anti-PGL-I ELISA OD values and resistance to leprosy and between IgM anti-PGL-I and leprosy progression or susceptibility. Serum PGL-I antigen levels, determined by dot ELISA, paralleled disease severity longitudinally. High positive OD values of anti-LAM IgG prior to ML inoculation were observed in the majority of leprosy-susceptible SMM in contrast to negative levels in more resistant animals. Anti-LAM IgG OD values exceeded the positive cut-off point after inoculation in 5 of 11 SMM; 3 of these 5 had concurrent detectable serum levels of PGL-I antigen.
BT - Leprosy review C1 - http://www.ncbi.nlm.nih.gov/pubmed/7637522?dopt=Abstract CN - Infolep Library - available DA - 1995 Jun DO - 10.5935/0305-7518.19950013 IS - 2 J2 - Lepr Rev LA - eng N2 -In this study, 11 SMM were grouped and inoculated with differing doses of SMM-origin Mycobacterium leprae (ML) between 4.5 x 10(8) and 1 x 10(9) by either combined IV/IC routes or by IV or IC route alone. The combined route was the most effective in eliciting progressive, disseminated LL leprosy. In all, 6 of 7 SMM inoculated by the combined routes developed leprosy requiring treatment at some point. Only 1 of 4 inoculated by a single route developed persisting leprosy requiring chemotherapy. Either no disease or spontaneous regression of initial disease occurred in the other 3 animals inoculated by a single route. Doses in excess of 1 x 10(9) ML were more effective than lesser doses. An association was observed between the development of IgG anti-PGL-I ELISA OD values and resistance to leprosy and between IgM anti-PGL-I and leprosy progression or susceptibility. Serum PGL-I antigen levels, determined by dot ELISA, paralleled disease severity longitudinally. High positive OD values of anti-LAM IgG prior to ML inoculation were observed in the majority of leprosy-susceptible SMM in contrast to negative levels in more resistant animals. Anti-LAM IgG OD values exceeded the positive cut-off point after inoculation in 5 of 11 SMM; 3 of these 5 had concurrent detectable serum levels of PGL-I antigen.
PY - 1995 SP - 105 EP - 25 T2 - Leprosy review TI - Experimental leprosy in monkeys. II. Longitudinal serological observations in sooty mangabey monkeys. UR - http://leprev.ilsl.br/pdfs/1995/v66n2/pdf/v66n2a03.pdf VL - 66 SN - 0305-7518 ER -