Inhibition of HIV-1 Infection by the β-Chemokine MDC
CD8$^+$ T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8$^+$ T cell clone and identified as...
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Published in | Science (American Association for the Advancement of Science) Vol. 278; no. 5338; pp. 695 - 698 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Society for the Advancement of Science
24.10.1997
American Association for the Advancement of Science The American Association for the Advancement of Science |
Subjects | |
Online Access | Get full text |
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Abstract | CD8$^+$ T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8$^+$ T cell clone and identified as the β-chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of CD8$^+$ cell-depleted peripheral blood mononuclear cells by primary non-syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line-adapted isolate HIV-1$_{IIIB}$. MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that β-chemokines are responsible for a major proportion of HIV-1-specific suppressor activity produced by primary T cells. |
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AbstractList | CD8$^+$ T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8$^+$ T cell clone and identified as the β-chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of CD8$^+$ cell-depleted peripheral blood mononuclear cells by primary non-syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line-adapted isolate HIV-1$_{IIIB}$. MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that β-chemokines are responsible for a major proportion of HIV-1-specific suppressor activity produced by primary T cells. CD8(+) T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8(+) T cell clone and identified as the beta-chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of CD8(+) cell-depleted peripheral blood mononuclear cells by primary non-syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line-adapted isolate HIV-1IIIB. MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that beta-chemokines are responsible for a major proportion of HIV-1-specific suppressor activity produced by primary T cells. [CD8.sup.+] T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized [CD8.sup.+] T cell clone and identified as the p-chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of [CD8.sup.+] cell-depleted peripheral blood mononuclear cells by primary non-syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line-adapted isolate [HIV-1.sub.IIIB]. MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that [Beta]-chemokines are responsible for a major proportion of HIV-1-specific suppressor activity produced by primary T cells. Scientific observations indicate that beta-chemokines are responsible for a major proportion of HIV-1-specific suppressor activity by primary T cells. CD8 super(+) T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8 super(+) T cell clone and identified as the beta -chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of CD8 super(+) cell-depleted peripheral blood mononuclear cells by primary non-syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line-adapted isolate HIV-1 sub(IIIB). MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that beta -chemokines are responsible for a major proportion of HIV-1-specific suppressor activity produced by primary T cells. CD8 + T lymphocytes from individuals infected with human immunodeficiency virus–type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8 + T cell clone and identified as the β-chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of CD8 + cell–depleted peripheral blood mononuclear cells by primary non–syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line–adapted isolate HIV-1 IIIB . MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that β-chemokines are responsible for a major proportion of HIV-1–specific suppressor activity produced by primary T cells. |
Audience | Academic |
Author | Pal, Ranajit Markham, Phillip D. Brown, Michelle Garzino-Demo, Alfredo Gallo, Robert C. DeVico, Anthony L. Burns, Jennifer |
Author_xml | – sequence: 1 givenname: Ranajit surname: Pal fullname: Pal, Ranajit – sequence: 2 givenname: Alfredo surname: Garzino-Demo fullname: Garzino-Demo, Alfredo – sequence: 3 givenname: Phillip D. surname: Markham fullname: Markham, Phillip D. – sequence: 4 givenname: Jennifer surname: Burns fullname: Burns, Jennifer – sequence: 5 givenname: Michelle surname: Brown fullname: Brown, Michelle – sequence: 6 givenname: Robert C. surname: Gallo fullname: Gallo, Robert C. – sequence: 7 givenname: Anthony L. surname: DeVico fullname: DeVico, Anthony L. |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2055100$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/9381181$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | Copyright 1997 American Association for the Advancement of Science 1998 INIST-CNRS COPYRIGHT 1997 American Association for the Advancement of Science COPYRIGHT 1997 American Association for the Advancement of Science Copyright American Association for the Advancement of Science Oct 24, 1997 |
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Keywords | Human HIV-1 virus Retroviridae Lentivirus Host virus relation Cell subpopulation Virus Chemokine Infectivity T-Lymphocyte Antiviral Human immunodeficiency virus Infected cell Inhibition |
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Snippet | CD8$^+$ T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1.... CD8(+) T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1.... CD8 + T lymphocytes from individuals infected with human immunodeficiency virus–type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A... [CD8.sup.+] T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by... CD8 super(+) T lymphocytes from individuals infected with human immunodeficiency virus-type 1 (HIV-1) secrete a soluble activity that suppresses infection by... Scientific observations indicate that beta-chemokines are responsible for a major proportion of HIV-1-specific suppressor activity by primary T cells. |
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SubjectTerms | AIDS/HIV Amino Acid Sequence Amino acids Antiviral Agents - immunology Biological and medical sciences Blotting, Northern Calcium - blood CD8-Positive T-Lymphocytes - immunology Cell Line Cell Line, Transformed Cell lines Cells, Cultured Cellular biology Chemokine CCL22 Chemokines Chemokines, CC - chemistry Chemokines, CC - immunology Chemokines, CC - isolation & purification Chemokines, CC - metabolism Cultured cells Cytokines Fractions Fundamental and applied biological sciences. Psychology HIV HIV (Viruses) HIV 1 HIV Core Protein p24 - biosynthesis HIV infection HIV infections HIV Infections - immunology HIV-1 - immunology HIV-1 - physiology Human immunodeficiency virus Humans Inactivation Infections Leukocytes, Mononuclear - immunology Leukocytes, Mononuclear - metabolism Leukocytes, Mononuclear - virology Lymphocyte Activation Microbiology Physiological aspects Prevention Receptors Receptors, Chemokine - metabolism Receptors, HIV - metabolism Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains RNA T cells T lymphocytes T-Lymphocytes - immunology Virology Virus inactivation Viruses |
Title | Inhibition of HIV-1 Infection by the β-Chemokine MDC |
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