Evidence map›Paper›PMID 2407653›Full record

ArticleInfection and immunity1990

Identification of an immunostimulating protein from Mycobacterium leprae.

N Mohagheghpour, M W Munn, R H Gelber, E G Engleman

Abstract read
In one paragraph

Article in Infection and immunity, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
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  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

N MohagheghpourDepartment of Pathology, Stanford University, California 94305.
M W Munn
R H Gelber
E G Engleman

Funding

IMMUNOLOGIC DEFECTS IN LEPROMATOUS LEPROSYR01AI022653 · NIAID · MEDICAL RESEARCH INSTITUTE OF SAN FRAN · PI MOHAGHEGHPOUR, NAHID · 1989 to 1991
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IMMUNOLOGIC DEFECTS IN LEPROMATOUS LEPROSYR22AI022653 · NIAID · STANFORD UNIVERSITY · PI MOHAGHEGHPOUR, NAHID · 1985 to 1991
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NIAID NIH HHS AI22653NIAID NIH HHS N0 1-AI-52582
6 · The paper itself

Abstract

Despite the recent identification of a number of Mycobacterium leprae proteins, the major immunogenic determinants of this organism remain obscure. We isolated from M. leprae a potent immunostimulatory preparation, designated the MLP fraction, which contains a major protein of 35 kilodaltons (kDa). This protein was precipitated by monoclonal antibody ML03-A1, which recognizes a 35-kDa protein of M. leprae, and by sera obtained from patients with lepromatous leprosy. Neither sera from healthy controls nor sera from patients with pulmonary tuberculosis recognized the 35-kDa protein, and only one of four serum samples from patients with borderline tuberculoid leprosy reacted with this protein. The MLP fraction stimulated T-cell proliferation in patients with leprosy whose T cells proliferate in response to whole M. leprae cells. Apparently, the T-cell epitope associated with MLP is also expressed on M. tuberculosis and M. bovis BCG, since patients with pulmonary tuberculosis and BCG-vaccinated individuals demonstrated significant responses to the MLP fraction. The 35-kDa M. leprae protein, purified to homogeneity in the laboratory of P. J. Brennan, stimulated T-cell proliferative responses in all MLP-responsive subjects. These findings suggest that the 35-kDa protein present in MLP is an immunostimulatory component of M. leprae. In addition to serving as a useful probe for study of the T-cell anergy associated with lepromatous disease, this protein may ultimately be useful as a component of a vaccine designed to provide protection against infection with M. leprae.

Indexed as

Adjuvants, ImmunologicBacterial ProteinsBacterial VaccinesElectrophoresis, Polyacrylamide GelHumansLymphocyte ActivationMolecular WeightMycobacterium lepraeT-LymphocytesAdjuvants, ImmunologicBacterial ProteinsBacterial Vaccines

Identifiers

PMID2407653
PMCPMC258522

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.