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Journal ArticleDOI

Serological profiles in Indian post kala-azar dermal leishmaniasis.

TLDR
Analysis of the data suggests an over-all difference between the serological profiles of PKADL and KA patients and reasonably good correlation between the severity of dermal lesions and IgG-ELISA titres was obtained.
Abstract
Post kala-azar dermal leishmaniasis (PKADL) is sequal to some of the visceral leishmaniasis (kala-azar) patients. More than 10% of Indian kala-azar (KA) patients develop this nonulcerative skin lesions, containing Leishmania donovani, within one to two years after recovery from visceral infection by the parasite (Brahmachari, 1922). The apparent change in the viscerotropic properties of L. donovani to dermatotropism is believed to be induced by the immunoregulatory mechanisms operating in these treated KA patients (Adler, 1964). Presence of antileishmanial antibodies were demonstrated in the sera of PKADL patients with active dermal lesions (Mukherjee et al., 1968, Haldar et al., 1981). Attention has been focussed on the cell-mediated immune (CMI) response (Haldar et al, 1983) as CMI plays a major role in protection against leishmaniasis (Mauel and Behin, 1982). In the present study, we have attempted to look into both the cellular and humoral immune profiles of 14 Indian PKADL patients, followed up longitudinally before and after the period of treatment. For this, lymphocyte transformation tests have been carried out in vitro in the presence of Leishmania antigen and the results are correlated with those of skin test experiments in vivo. Furthermore, alterations in the serum IgG and IgM class specific antileishmanial antibody titers have been determined by standardized ELISA method. All these results are discussed with respect to our knowledge on the immunology of clinical leishmaniasis.

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Citations
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Journal ArticleDOI

Laboratory Diagnosis of Visceral Leishmaniasis

TL;DR: The group of diseases known as the leishmaniases are caused by obligate intracellular protozoa of the genus Leishmania.
Journal ArticleDOI

Serodiagnosis of Leishmaniasis

TL;DR: The use of whole promastigote as the source of antigens in the direct agglutination test (DAT) and immunofluorescent test (IFAT) gave cross-reactions with the sera of leprosy, tuberculosis, and African trypanosomiasis patients.
Journal ArticleDOI

Cell-mediated immune response in Indian kala-azar and post-kala-azar dermal leishmaniasis.

TL;DR: It is suggested that the protection afforded by specific CMI response against Leishmania donovani infection may not be absolute and probably depends on other host-related factors leading to parasite destruction and patient recovery.
Journal ArticleDOI

Diagnosis of visceral leishmaniasis: developments over the last decade

TL;DR: Improvement in VL diagnostics is required for successful decentralized testing in field conditions and to detect VL–HIV co-infection and the diagnosis based on bioanalytics/biosensors promise frontiers for point-of-care VL detection after adequate standardization.
Journal Article

Visceral leishmaniasis (kala-azar): Challenges ahead

TL;DR: There is a pressing need for the technological advancement in the understanding of immune response, drug resistance and the pathogenesis of leishmaniasis that could be translated into field applicable and affordable methods for diagnosis, treatment, and control of the disease.
References
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Journal ArticleDOI

Immunochemical quantitation of antigens by single radial immunodiffusion

TL;DR: By standardizing the technical conditions of the experiment it is possible to use this principle for the immunochemical determination of antigens, and the lower limit of the method was found to correspond to 0·0025 μg of antigen, and to an antigen concentrations of 1·25 μg per ml.
Journal ArticleDOI

The glomerular permeability determined by dextran clearance using Sephadex gel filtration.

TL;DR: A method is described for measuring glomerular permeability by dextran clearance using Sephadex gel filtration technique, and clearance is shown to be a function of molecular size, decreasing with increasing molecular weight.
Journal ArticleDOI

Enzyme immunoassays for parasitic diseases.

TL;DR: Serology has come to play a major role in parasitic diseases and enzyme-immunoassays, especially the enzyme-linked immunosorbent assay, have a part to play in both the above situations.
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