Detection of Phenolic Glycolipid I of Mycobacterium leprae in Sera from Leprosy Patients before and after Start of Multidrug Therapy

Author:

Cho Sang-Nae12,Cellona Roland V.3,Villahermosa Laarni G.3,Fajardo Tranquilino T.3,Balagon M. Victoria F.3,Abalos Rodolfo M.3,Tan Esterlina V.3,Walsh Gerald P.3,Kim Joo-Deuk12,Brennan Patrick J.4

Affiliation:

1. Department of Microbiology1 and

2. Institute for Immunology and Immunological Diseases,2 Yonsei University College of Medicine, Seoul 120-752, The Republic of Korea;

3. Leonard Wood Memorial Center, Cebu 6000, The Philippines3; and

4. Department of Microbiology, Colorado State University, Fort Collins, Colorado 805234

Abstract

ABSTRACT A total of 100 untreated new leprosy patients were recruited prospectively and examined for the presence of phenolic glycolipid I (PGL-I) antigen in their serum specimens by dot enzyme-linked immunosorbent assay (ELISA) using rabbit anti-PGL-I antiserum. The presence of circulating PGL-I antigen was closely related to the bacterial indices (BI) of the patients. The PGL-I antigen was detectable in 27 (93.1%) of 29 patients with a BI of 4.0 or above and in 15 (68.2%) of 22 patients with a BI of 3.0 to 3.9. However, none of the 37 patients with a BI of less than 1.9 had detectable PGL-I antigen by the methods used in this study. The level of PGL-I in serum declined rapidly by about 90% 1 month after the start of multidrug therapy. This study showed clearly that anti-PGL-I IgM antibodies and circulating PGL-I antigen levels reflect the bacterial loads in untreated leprosy patients. The serological parameters based on the PGL-I antigen may therefore be useful in the assessment of leprosy patients at the time of diagnosis and possibly in monitoring patients following chemotherapy.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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