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 inScience (American Association for the Advancement of Science) Vol. 278; no. 5338; pp. 695 - 698
Main Authors Pal, Ranajit, Garzino-Demo, Alfredo, Markham, Phillip D., Burns, Jennifer, Brown, Michelle, Gallo, Robert C., DeVico, Anthony L.
Format Journal Article
LanguageEnglish
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
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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.
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
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  givenname: Phillip D.
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  surname: DeVico
  fullname: DeVico, Anthony L.
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ContentType Journal Article
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IsPeerReviewed true
IsScholarly true
Issue 5338
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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jstor
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StartPage 695
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
URI https://www.jstor.org/stable/2901176
https://www.ncbi.nlm.nih.gov/pubmed/9381181
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https://search.proquest.com/docview/16229488
https://search.proquest.com/docview/743709972
https://search.proquest.com/docview/79381149
Volume 278
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