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Featured researches published by Sengupta U.


Leprosy Review | 1991

Association of mycobacterial-specific and Mycobacterium leprae specific antibody levels with clinical activity in tuberculoid leprosy : a comparative study of three serological enzyme-immunoassays

Vinita Chaturvedi; Sudhir Sinha; Girdhar Bk; Kiran Katoch; A. S. Bhatia; Sengupta U

The ELISAs for polyclonal antibodies against Mycobacterium leprae (ML-ELISA) and specific antibodies against epitopes on 35 kDa protein (SACT-ELISA) and phenolic glycolipid I (PG-ELISA) of M. leprae were evaluated comparatively in a group of 88 tuberculoid leprosy patients. The overall seropositivity rate with a battery of 3 tests (68%) was not significantly higher than that obtained with ML-ELISA alone (55%) for IgG class of antibodies. Seropositivities for SACT-ELISA and PG-ELISA were, respectively, 38% and 26%. ML-ELISA for IgM class of antibodies was least sensitive, showing only 8% positivity. A significant correlation was noted between individual values of the three assays, but the positive proportions overlapped maximally in the case of ML-ELISA (IgG) and SACT-ELISA. Further, positivity for the latter two assays, particularly SACT-ELISA, showed significant associations with the extent of active (largely untreated) infection. Immunoblotting revealed that the main antibody response was directed towards M. leprae antigens in the molecular weight range of 20-40 kDa and the densitometry results of this zone correlated significantly with corresponding SACT-ELISA and ML-ELISA (IgG) values.


Immunology Letters | 1990

In situ demonstration of Mycobacterium leprae antigens in leprosy lesions using monoclonal antibodies

R.B. Narayanan; B.K. Girdhar; Malaviya Gn; Sengupta U

Cryostat sections of skin and nerve lesions of leprosy were stained with monoclonal antibodies recognising Mycobacterium leprae antigens and indirect immunofluorescence. In both the tuberculoid and lepromatous lesions, PGL1, 55-65-kDa, 17-kDa protein antigens and cross-reactive non-protein antigens were present. 65-kDa antigens were seen mainly in the skin lesions of lepromatous leprosy. The infiltrates in both the skin and nerve granulomas of tuberculoid and lepromatous leprosy showed membranous staining with monoclonal antibodies recognising PGL1 and 55-65-kDa antigens. Bacilli in the lesions and the cells in the lymph node granulomas of patients with tuberculosis or the infiltrates in the lesions of tinea corporis or sections of normal skin did not show any staining with these monoclonal antibodies. These results confirm that M. leprae antigens are present and are expressed on the infiltrating cells of leprosy lesions.


Journal of Biosciences | 1990

Coupling of proteins to liposomes and their role in understanding delayed type of hypersensitivity in human and mice

Sengupta U; Sudhir Sinha; V. Chaturvedi; R.B. Narayanan; Sreevatsa; C. M. Gupta

AbstractsLiposome-coupled lepromin was found to elicit a 3-week skin reaction in leprosy patients similar to that elicited by wholeMycobacterium leprae. The present study suggests that the presentation of antigens in a specific orientation is necessary for evoking delayed type hypersensitivity response in humans.


International Archives of Allergy and Immunology | 1987

Immunohistologic Comparison between Armadillo-Derived Leprosin and Standard Lepromin Skin Tests in Leprosy Patients

R.B. Narayanan; G. Ramu; S. Sinha; Sengupta U; C.M. Gupta

A comparison was made on the in situ immunological characteristics of dermal infiltrates of early (24-hour) and late (3-4 weeks) skin reactions in leprosy patients. The skin reactions were induced by armadillo-derived leprosin coupled to liposomes and standard Dharmendra lepromin. Most lymphocytes in the early reaction induced by both antigens were positive for Leu 4, Leu 3a, OKT8 and Ia like antigens indicating thereby the presence of activated T cells. The ratio of Leu 3a/OKT8+ cells were similar. In the late reaction elicited by both antigens, the lymphocytes in the granulomas were predominantly activated T lymphocytes expressing Leu 4, Leu 3a, OKT8 and Ia like antigens. Leu 3a+ cells were scattered diffusely amidst the epithelioid cells. In contrast, the OKT8+ cells were present mainly as a ring in the periphery of the granuloma. A similar ratio of Leu 3a+/OKT8+ cells was observed in these granulomas. Macrophages in the granulomas expressed Ia like antigens. These observations indicate that the immunological characteristics of dermal infiltrates in the skin reaction induced by armadillo-derived leprosin coupled to liposomes and standard Dharmendra lepromin appear to be identical.


Archive | 1989

Serological Survey of Leprosy Using a Monoclonal Antibody-Based Immunoassay and Phenolic Glycolipid ELISA

Sengupta U; Sudhir Sinha; S. A. Patil; Girdhar Bk; Ramu G

The present global estimate of leprosy patients is 11.5 million (21), one- fourth of whom live in India (6). The spread of infection can be arrested effectively by diagnosis and treatment of infectious subjects at an early (“preclinical”) stage (21). However, the available diagnostic tools are often inadequate for this purpose. Three of the Mycobacterium leprae-specific serological tests—the fluorescent leprosy-antibody absorption test (FLA- ABS), the phenolic glycolipid I-based enzyme-linked immunosorbent assay (PG-ELISA) and a monoclonal antibody—serum antibody competition test (SACT) have shown promising results when applied to the study of healthy contacts of leprosy patients (1,3,8,17,19). The present review is mainly attributed to the work done using SACT.


International Archives of Allergy and Immunology | 1989

CD1-positive epidermal Langerhans cells in skin reactions to autologous peripheral-blood-derived mononuclear cells in leprosy patients

R.B. Narayanan; M. Natarajan; Katoch K; Sengupta U

A comparison was made on the characteristics of the infiltrates, the number and distribution of CD1-positive epidermal Langerhans cells (LC) at the sites of skin reaction induced by autologous peripheral-blood-derived mononuclear cells (PBMC) in leprosy patients. Clinically and histologically, the skin reaction was well expressed in tuberculoid patients as compared to lepromatous patients, erythema nodosum leprosum (ENL) patients and contacts. The quantum of lymphocytes in the infiltrates was maximal in the tuberculoid patients and it was minimal in lepromatous and ENL patients. The number and distribution of LC in the tuberculoid patients was significantly higher in the PBMC-inoculated sites as compared to control sites over 24 h. In contrast, no difference in the number and distribution of LC was noticed in the lepromatous and ENL patients. These observations indicate that the lymphocytes of tuberculoid patients in contrast to lepromatous leprosy patients are capable of sustenance in the local micro-environments of the skin and an effective interaction may be possible between LC and PBMC.


International Journal of Leprosy and Other Mycobacterial Diseases | 1991

A clinical, immunological, and histological study of neuritic leprosy patients

Kaur G; Girdhar Bk; Girdhar A; Malaviya Gn; Mukherjee A; Sengupta U; Desikan Kv


International Journal of Leprosy and Other Mycobacterial Diseases | 1985

Serological survey of leprosy and control subjects by a monoclonal antibody-based immunoassay.

Sudhir Sinha; Sengupta U; Ramu G; Ivanyi J


International Journal of Leprosy and Other Mycobacterial Diseases | 2005

Seroprevalence of HIV infection among leprosy patients in Agra, India: trends and perspective.

Tahziba Hussain; Shikha Sinha; K.K. Kulshreshtha; Katoch K; V.S. Yadav; Sengupta U; Katoch Vm


International Journal of Leprosy and Other Mycobacterial Diseases | 2000

HIV seroprevalence in leprosy patients.

Tahziba Hussain; K. Kulshreshtha; S. K. Ghei; M. Natarajan; Katoch K; Sengupta U

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Sudhir Sinha

Central Drug Research Institute

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Girdhar Bk

Indian Council of Medical Research

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Malaviya Gn

Indian Council of Medical Research

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B.K. Girdhar

Indian Council of Medical Research

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Tahziba Hussain

Indian Council of Medical Research

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Vinita Chaturvedi

Central Drug Research Institute

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C.M. Gupta

Central Drug Research Institute

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G. Ramu

Indian Council of Medical Research

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K.K. Kulshreshtha

Indian Council of Medical Research

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