Evidence map›Paper›PMID 8358707›Full record

ReviewClinical microbiology reviews1993

The Mycobacterium avium complex.

C B Inderlied, C A Kemper, L E Bermudez

Open access · greenAbstract readReview
In one paragraph

Review in Clinical microbiology reviews, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 236 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
236citing papers in PubMed, 2 pooled it
26.8field-weighted citation impact, top 1% of its field
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

236 citing papers in PubMed, 2 syntheses or guidelines pooled it, 671 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Microbiology (Reading, England) · 2026
    Article
  7. Article
  8. bioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. TheMicroorganisms · 2025
    Review
  11. Article
  12. Frontiers in immunology · 2025
    Article
  13. Article
  14. Review
  15. Detection of theIranian journal of veterinary research · 2023
    Article
  16. Diagnosis ofFrontiers in medicine · 2023
    Article
  17. Article
  18. Article
  19. High rate of reinfection and possible transmission ofOne health (Amsterdam, Netherlands) · 2022
    Article
  20. Article

176 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

C B InderliedDepartment of Pathology and Laboratory Medicine, Childrens Hospital, Los Angeles, California 90027.
C A Kemper
L E Bermudez
Children's Hospital of Los Angeles · US

Funding

EVALUATION OF THERAPIES FOR MYOBACTERIUM AVIUMN01AI025140 · NIAID · CALIFORNIA PACIFIC MED CTR RES INSTITUTE · PI YOUNG, LOWELL S. · 1992 to 1998
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REFERENCE LAB FOR NON-TB MYCOBACTERIAN01AI025146 · NIAID · CHILDREN'S HOSPITAL LOS ANGELES · PI INDERLIED, CLARK B · 1992 to 1998
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PATHOGENESIS &HOST DEFENSE AGAINST M. AVIUMR01AI025769 · NIAID · MEDICAL RESEARCH INSTITUTE OF SAN FRAN · PI YOUNG, LOWELL S. · 1987 to 1994
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NIAID NIH HHS AI 25140NIAID NIH HHS AI 25146NIAID NIH HHS AI 25769
6 · The paper itself

Abstract

Mycobacterium avium complex (MAC) disease emerged early in the epidemic of AIDS as one of the common opportunistic infections afflicting human immunodeficiency virus-infected patients. However, only over the past few years has a consensus developed about its significance to the morbidity and mortality of AIDS. M. avium was well known to mycobacteriologists decades before AIDS, and the MAC was known to cause disease, albeit uncommon, in humans and animals. The early interest in the MAC provided a basis for an explosion of studies over the past 10 years largely in response to the role of the MAC in AIDS opportunistic infection. Molecular techniques have been applied to the epidemiology of MAC disease as well as to a better understanding of the genetics of antimicrobial resistance. The interaction of the MAC with the immune system is complex, and putative MAC virulence factors appear to have a direct effect on the components of cellular immunity, including the regulation of cytokine expression and function. There now is compelling evidence that disseminated MAC disease in humans contributes to both a decrease in the quality of life and survival. Disseminated disease most commonly develops late in the course of AIDS as the CD4 cells are depleted below a critical threshold, but new therapies for prophylaxis and treatment offer considerable promise. These new therapeutic modalities are likely to be useful in the treatment of other forms of MAC disease in patients without AIDS. The laboratory diagnosis of MAC disease has focused on the detection of mycobacteria in the blood and tissues, and although the existing methods are largely adequate, there is need for improvement. Indeed, the successful treatment of MAC disease clearly will require an early and rapid detection of the MAC in clinical specimens long before the establishment of the characteristic overwhelming infection of bone marrow, liver, spleen, and other tissue. Also, a standard method of susceptibility testing is of increasing interest and importance as new effective antimicrobial agents are identified and evaluated. Antimicrobial resistance has already emerged as an important problem, and methods for circumventing resistance that use combination therapies are now being studied.

Indexed as

Mycobacterium avium-intracellulare InfectionAIDS-Related Opportunistic InfectionsAnimalsHumansImmunity, CellularMycobacterium avium Complex

Identifiers

PMID8358707
PMCPMC358286
OpenAlexW2155186392

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.