Evidence map›Paper›PMID 9847379›Full record

ArticleJournal of virology1999

Intrinsic human immunodeficiency virus type 1 resistance of hematopoietic stem cells despite coreceptor expression.

H Shen, T Cheng, F I Preffer, D Dombkowski, M H Tomasson, D E Golan, O Yang, W Hofmann, J G Sodroski, A D Luster and 1 more

Abstract read
In one paragraph

Article in Journal of virology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
–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

45 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Antiviral resistance of stem cells.Current opinion in immunology · 2019
    Review
  10. Review
  11. Article
  12. Prostaglandin EMolecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. HIV-1 pathogenesis: the virus.Cold Spring Harbor perspectives in medicine · 2012
    Article
  20. Article
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

11 authors.

H ShenAIDS Research Center, MGH Cancer Center, Divisions of Infectious Diseases and Hematology/Oncology, Massachusetts General Hospital, Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
T Cheng
F I Preffer
D Dombkowski
M H Tomasson
D E Golan
O Yang
W Hofmann
J G Sodroski
A D Luster
D T Scadden

Funding

TRANSPLANTATION IN MODELS OF GENETIC DISEASEP50HL054785 · NHLBI · DANA-FARBER CANCER INSTITUTE · PI NATHAN, DAVID G. · 1995 to 2004
$8.8M
Multidisciplinary HIV Training ProgramT32AI007387 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Daniel R. Kuritzkes · 1990 to 2026
$8.8M
MECHANISMS OF HEMATOPOIESIS IN AIDSR01HL044851 · NHLBI · NEW ENGLAND DEACONESS HOSPITAL · PI SCADDEN, DAVID T · 1991 to 2015
$7.7M
Molecular Interactions in Erythroid Cell MembranesR37HL032854 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GOLAN, DAVID E. · 1997 to 2006
$3.0M
Molecular Regulation of Adhesive Integrin Interactions in Erythroblastic IslandsR01HL032854 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GOLAN, DAVID E. · 1985 to 2011
$2.0M
COMPARATIVE BIOLOGY OF HEMATOPOIETIC STEM CELLSR01HL055718 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SCADDEN, DAVID T · 1995 to 1999
–
NHLBI NIH HHS HL 32854NHLBI NIH HHS HL 44851NHLBI NIH HHS HL 55718NHLBI NIH HHS P50 HL054785NHLBI NIH HHS R01 HL032854NHLBI NIH HHS R01 HL044851NHLBI NIH HHS R37 HL032854NIAID NIH HHS T32 AI007387
6 · The paper itself

Abstract

Interactions of human immunodeficiency virus type 1 (HIV-1) with hematopoietic stem cells may define restrictions on immune reconstitution following effective antiretroviral therapy and affect stem cell gene therapy strategies for AIDS. In the present study, we demonstrated mRNA and cell surface expression of HIV-1 receptors CD4 and the chemokine receptors CCR-5 and CXCR-4 in fractionated cells representing multiple stages of hematopoietic development. Chemokine receptor function was documented in subsets of cells by calcium flux in response to a cognate ligand. Productive infection by HIV-1 via these receptors was observed with the notable exception of stem cells, in which case the presence of CD4, CXCR-4, and CCR-5, as documented by single-cell analysis for expression and function, was insufficient for infection. Neither productive infection, transgene expression, nor virus entry was detectable following exposure of stem cells to either wild-type HIV-1 or lentivirus constructs pseudotyped in HIV-1 envelopes of macrophage-tropic, T-cell-tropic, or dualtropic specificity. Successful entry into stem cells of a vesicular stomatitis virus G protein-pseudotyped HIV-1 construct demonstrated that the resistance to HIV-1 was mediated at the level of virus-cell membrane fusion and entry. These data define the hematopoietic stem cell as a sanctuary cell which is resistant to HIV-1 infection by a mechanism independent of receptor and coreceptor expression that suggests a novel means of cellular protection from HIV-1.

Indexed as

Acquired Immunodeficiency SyndromeAdultAntigens, CD34CD4 AntigensGenetic TherapyHematopoietic Stem CellsHIV-1HumansReceptors, CCR5Receptors, CXCR4RNA, MessengerAntigens, CD34CD4 AntigensReceptors, CCR5Receptors, CXCR4RNA, Messenger

Identifiers

PMID9847379
PMCPMC103880

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.