01683nas a2200325 4500000000100000008004100001260001300042653001200055653002600067653002500093653002200118653002500140653002000165653003200185653001100217653001000228653002400238653002800262653002000290100001300310700001100323700001400334700001300348700001500361245007200376300001100448490000700459520087700466022001401343 1995 d c1995 Nov10aAnimals10aAntibodies, Protozoan10aAntibody Specificity10aBlotting, Western10aCase-Control Studies10aCross Reactions10aEvaluation Studies as Topic10aHumans10aIndia10aLeishmania donovani10aLeishmaniasis, Visceral10aSerologic Tests1 aTiwari V1 aJain A1 aAgarwal M1 aMittal B1 aPandey H P00aEvaluation of antibody responses in Indian kala-azar by immunoblot. a959-640 v373 a

When infected with Leishmania species, patients develop specific antibodies that constitute the basis of serodiagnosis. using Western blot analysis we studied the specificity of anti-leishmania donovani antibodies in patients with visceral leishmaniasis, healthy subjects living in an endemic and non-endemic areas, and patients of other infectious diseases like malaria, leprosy, tuberculosis and tropical splenomegaly. Sera from patients with kala-azar recognised numerous antigens that had a molecular weight of 150 KD, 145 KD, 120 KD, 92 KD, 87 KD, 72 KD, 65 KD, 56 KD, 50 KD, 40 KD, 26 KD, 21 KD, 14 KD, AND 12 KD. The 150, 145, 120, 92, 87, 81, 65, 25, 21, 14, and 12 KD antigens had the greatest specificity for kala-azar sera while the bands of molecular weights 72, 56, 50, and 40 KD were found to be cross reactive with sera of patients of other diseases.

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