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Sequential monitoring of leprosy patients with serum antibody levels to phenolic glycolipid-I, a synthetic analog of phenolic glycolipid-I, and mycobacterial lipoarabinomannan.
Int J Lepr Other Mycobact Dis. 1990 Sep; 58(3):503-11.IJ

Abstract

Sequential serum samples from leprosy patients at various stages of antibacterial treatment were tested by an ELISA for antibodies to phenolic glycolipid I (PGL-I), a synthetic PGL-I analog (ND-BSA), and lipoarabinomannan (LAM) from Mycobacterium tuberculosis to determine if these antibodies could be useful in monitoring response to therapy. Among patients with positive initial anti-PGL-I IgM, a significant decrease in this antibody was seen over time (p less than 0.01), whether assayed by PGL-I or ND-BSA. The two antigens showed good agreement in the detection of decrease in anti-PGL-I IgM. The greatest decrease was seen in patients with a high initial anti-PGL-I IgM and a high bacterial index (BI). Patients with a declining BI were seen to have generally declining antibody levels to PGL-I and to LAM; in those patients with a fluctuating BI, antibody levels were less predictable. We conclude that antibodies to PGL-I and LAM can be useful in following response to therapy in leprosy patients and that either the native PGL-I or ND-BSA can serve as antigen for the ELISA.

Authors+Show Affiliations

New York State Institute for Basic Research in Developmental Disabilities, Staten Islan 10314.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

2205685

Citation

Meeker, H C., et al. "Sequential Monitoring of Leprosy Patients With Serum Antibody Levels to Phenolic glycolipid-I, a Synthetic Analog of Phenolic glycolipid-I, and Mycobacterial Lipoarabinomannan." International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association, vol. 58, no. 3, 1990, pp. 503-11.
Meeker HC, Schuller-Levis G, Fusco F, et al. Sequential monitoring of leprosy patients with serum antibody levels to phenolic glycolipid-I, a synthetic analog of phenolic glycolipid-I, and mycobacterial lipoarabinomannan. Int J Lepr Other Mycobact Dis. 1990;58(3):503-11.
Meeker, H. C., Schuller-Levis, G., Fusco, F., Giardina-Becket, M. A., Sersen, E., & Levis, W. R. (1990). Sequential monitoring of leprosy patients with serum antibody levels to phenolic glycolipid-I, a synthetic analog of phenolic glycolipid-I, and mycobacterial lipoarabinomannan. International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association, 58(3), 503-11.
Meeker HC, et al. Sequential Monitoring of Leprosy Patients With Serum Antibody Levels to Phenolic glycolipid-I, a Synthetic Analog of Phenolic glycolipid-I, and Mycobacterial Lipoarabinomannan. Int J Lepr Other Mycobact Dis. 1990;58(3):503-11. PubMed PMID: 2205685.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Sequential monitoring of leprosy patients with serum antibody levels to phenolic glycolipid-I, a synthetic analog of phenolic glycolipid-I, and mycobacterial lipoarabinomannan. AU - Meeker,H C, AU - Schuller-Levis,G, AU - Fusco,F, AU - Giardina-Becket,M A, AU - Sersen,E, AU - Levis,W R, PY - 1990/9/1/pubmed PY - 1990/9/1/medline PY - 1990/9/1/entrez SP - 503 EP - 11 JF - International journal of leprosy and other mycobacterial diseases : official organ of the International Leprosy Association JO - Int J Lepr Other Mycobact Dis VL - 58 IS - 3 N2 - Sequential serum samples from leprosy patients at various stages of antibacterial treatment were tested by an ELISA for antibodies to phenolic glycolipid I (PGL-I), a synthetic PGL-I analog (ND-BSA), and lipoarabinomannan (LAM) from Mycobacterium tuberculosis to determine if these antibodies could be useful in monitoring response to therapy. Among patients with positive initial anti-PGL-I IgM, a significant decrease in this antibody was seen over time (p less than 0.01), whether assayed by PGL-I or ND-BSA. The two antigens showed good agreement in the detection of decrease in anti-PGL-I IgM. The greatest decrease was seen in patients with a high initial anti-PGL-I IgM and a high bacterial index (BI). Patients with a declining BI were seen to have generally declining antibody levels to PGL-I and to LAM; in those patients with a fluctuating BI, antibody levels were less predictable. We conclude that antibodies to PGL-I and LAM can be useful in following response to therapy in leprosy patients and that either the native PGL-I or ND-BSA can serve as antigen for the ELISA. SN - 0148-916X UR - https://www.unboundmedicine.com/medline/citation/2205685/Sequential_monitoring_of_leprosy_patients_with_serum_antibody_levels_to_phenolic_glycolipid_I_a_synthetic_analog_of_phenolic_glycolipid_I_and_mycobacterial_lipoarabinomannan_ DB - PRIME DP - Unbound Medicine ER -