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.
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 -