Diagnostik af HIV-1 infektionen

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Diagnostik af HIV-1 infektionen. / Christiansen, C B; Dickmeiss, E; Bygbjerg, Ib Christian.

In: Ugeskrift for Laeger, Vol. 153, No. 35, 26.08.1991, p. 2410-4.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Christiansen, CB, Dickmeiss, E & Bygbjerg, IC 1991, 'Diagnostik af HIV-1 infektionen', Ugeskrift for Laeger, vol. 153, no. 35, pp. 2410-4.

APA

Christiansen, C. B., Dickmeiss, E., & Bygbjerg, I. C. (1991). Diagnostik af HIV-1 infektionen. Ugeskrift for Laeger, 153(35), 2410-4.

Vancouver

Christiansen CB, Dickmeiss E, Bygbjerg IC. Diagnostik af HIV-1 infektionen. Ugeskrift for Laeger. 1991 Aug 26;153(35):2410-4.

Author

Christiansen, C B ; Dickmeiss, E ; Bygbjerg, Ib Christian. / Diagnostik af HIV-1 infektionen. In: Ugeskrift for Laeger. 1991 ; Vol. 153, No. 35. pp. 2410-4.

Bibtex

@article{3ae54186c1f54e77bfa8c2f749de79a3,
title = "Diagnostik af HIV-1 infektionen",
abstract = "Different methods have been developed for the diagnosis of HIV infection, i.e. detection of antibodies, antigen and proviral DNA. ELISA methods for detecting HIV-1 antibodies are widely used as screening assays. A sample which is repeatedly positive with ELISA is re-tested with a confirmatory test, e.g. western blot. Antibodies to HIV-1 are not detectable until 2-3 months after infection, but antigens may be detectable during the last weeks of this initial period, though they disappear with the appearance of the antibodies. In the later stages of HIV infection, HIV antigen is again detectable in a proportion of patients. Detection and quantitation of HIV antigen are used as indicators of disease progression and for monitoring the antiviral efficacy of therapeutic interventions. When no antibodies or antigens can be detected in persons suspected of having HIV infection, culture of HIV can be performed. For research purposes, detection of small amounts of proviral DNA can be made with polymerase chain reaction (PCR). The method is not yet applicable in routine diagnosis of HIV infection.",
keywords = "Acquired Immunodeficiency Syndrome, Enzyme-Linked Immunosorbent Assay, HIV Infections, HIV Seropositivity, HIV-1, Humans, Immunoblotting, Immunologic Tests, Polymerase Chain Reaction",
author = "Christiansen, {C B} and E Dickmeiss and Bygbjerg, {Ib Christian}",
year = "1991",
month = aug,
day = "26",
language = "Dansk",
volume = "153",
pages = "2410--4",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "35",

}

RIS

TY - JOUR

T1 - Diagnostik af HIV-1 infektionen

AU - Christiansen, C B

AU - Dickmeiss, E

AU - Bygbjerg, Ib Christian

PY - 1991/8/26

Y1 - 1991/8/26

N2 - Different methods have been developed for the diagnosis of HIV infection, i.e. detection of antibodies, antigen and proviral DNA. ELISA methods for detecting HIV-1 antibodies are widely used as screening assays. A sample which is repeatedly positive with ELISA is re-tested with a confirmatory test, e.g. western blot. Antibodies to HIV-1 are not detectable until 2-3 months after infection, but antigens may be detectable during the last weeks of this initial period, though they disappear with the appearance of the antibodies. In the later stages of HIV infection, HIV antigen is again detectable in a proportion of patients. Detection and quantitation of HIV antigen are used as indicators of disease progression and for monitoring the antiviral efficacy of therapeutic interventions. When no antibodies or antigens can be detected in persons suspected of having HIV infection, culture of HIV can be performed. For research purposes, detection of small amounts of proviral DNA can be made with polymerase chain reaction (PCR). The method is not yet applicable in routine diagnosis of HIV infection.

AB - Different methods have been developed for the diagnosis of HIV infection, i.e. detection of antibodies, antigen and proviral DNA. ELISA methods for detecting HIV-1 antibodies are widely used as screening assays. A sample which is repeatedly positive with ELISA is re-tested with a confirmatory test, e.g. western blot. Antibodies to HIV-1 are not detectable until 2-3 months after infection, but antigens may be detectable during the last weeks of this initial period, though they disappear with the appearance of the antibodies. In the later stages of HIV infection, HIV antigen is again detectable in a proportion of patients. Detection and quantitation of HIV antigen are used as indicators of disease progression and for monitoring the antiviral efficacy of therapeutic interventions. When no antibodies or antigens can be detected in persons suspected of having HIV infection, culture of HIV can be performed. For research purposes, detection of small amounts of proviral DNA can be made with polymerase chain reaction (PCR). The method is not yet applicable in routine diagnosis of HIV infection.

KW - Acquired Immunodeficiency Syndrome

KW - Enzyme-Linked Immunosorbent Assay

KW - HIV Infections

KW - HIV Seropositivity

KW - HIV-1

KW - Humans

KW - Immunoblotting

KW - Immunologic Tests

KW - Polymerase Chain Reaction

M3 - Tidsskriftartikel

C2 - 1949239

VL - 153

SP - 2410

EP - 2414

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 35

ER -

ID: 33890898