Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells. / Søndergaard, S R; Ullum, H; Pedersen, Bente Klarlund.

In: APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, Vol. 108, No. 12, 12.2000, p. 831-7.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Søndergaard, SR, Ullum, H & Pedersen, BK 2000, 'Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells', APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, vol. 108, no. 12, pp. 831-7.

APA

Søndergaard, S. R., Ullum, H., & Pedersen, B. K. (2000). Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 108(12), 831-7.

Vancouver

Søndergaard SR, Ullum H, Pedersen BK. Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica. 2000 Dec;108(12):831-7.

Author

Søndergaard, S R ; Ullum, H ; Pedersen, Bente Klarlund. / Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells. In: APMIS : acta pathologica, microbiologica, et immunologica Scandinavica. 2000 ; Vol. 108, No. 12. pp. 831-7.

Bibtex

@article{80992efd73204422816dab440242f4ee,
title = "Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells",
abstract = "Natural killer (NK) cells can be divided into several subpopulations according to their expression of the surface antigens CD16 and CD56. The modest quantity of NK cells in the blood available for functional analysis has been a limitation in studies of NK cell subpopulations. In the present study, epinephrine infusion was used to induce lymphocytosis before immunomagnetic methods were applied to isolate CD16+/-CD56+ and CD16+CD56- CD3- NK cells. These subpopulations were compared according to their proliferative and cytotoxic capabilities in 10 human immunodeficiency virus (HIV)-infected individuals and 5 healthy controls. The CD16+CD56- NK cell subgroup had a higher proliferative capacity, whereas the CD16+/-CD56+ NK cell subgroup was mainly cytotoxic, and unaffected by HIV serostatus. This study thus suggests that NK cell phenotypes more strongly predict NK cell function than HIV serostatus. This assertion should be considered when studying NK cell function in subjects with a deviating composition of NK cells.",
keywords = "Adrenergic beta-Agonists, Adult, Antigens, CD56, Biomarkers, Cell Division, Cell Movement, Cytotoxicity, Immunologic, Epinephrine, Flow Cytometry, HIV Infections, HIV Seronegativity, Humans, Immunophenotyping, Killer Cells, Natural, Leukocyte Count, Lymphocytosis, Male, Receptors, IgG, Comparative Study, Journal Article, Research Support, Non-U.S. Gov't",
author = "S{\o}ndergaard, {S R} and H Ullum and Pedersen, {Bente Klarlund}",
year = "2000",
month = dec,
language = "English",
volume = "108",
pages = "831--7",
journal = "A P M I S. Acta Pathologica, Microbiologica et Immunologica Scandinavica",
issn = "0903-4641",
publisher = "Wiley Online",
number = "12",

}

RIS

TY - JOUR

T1 - Proliferative and cytotoxic capabilities of CD16+CD56- and CD16+/-CD56+ natural killer cells

AU - Søndergaard, S R

AU - Ullum, H

AU - Pedersen, Bente Klarlund

PY - 2000/12

Y1 - 2000/12

N2 - Natural killer (NK) cells can be divided into several subpopulations according to their expression of the surface antigens CD16 and CD56. The modest quantity of NK cells in the blood available for functional analysis has been a limitation in studies of NK cell subpopulations. In the present study, epinephrine infusion was used to induce lymphocytosis before immunomagnetic methods were applied to isolate CD16+/-CD56+ and CD16+CD56- CD3- NK cells. These subpopulations were compared according to their proliferative and cytotoxic capabilities in 10 human immunodeficiency virus (HIV)-infected individuals and 5 healthy controls. The CD16+CD56- NK cell subgroup had a higher proliferative capacity, whereas the CD16+/-CD56+ NK cell subgroup was mainly cytotoxic, and unaffected by HIV serostatus. This study thus suggests that NK cell phenotypes more strongly predict NK cell function than HIV serostatus. This assertion should be considered when studying NK cell function in subjects with a deviating composition of NK cells.

AB - Natural killer (NK) cells can be divided into several subpopulations according to their expression of the surface antigens CD16 and CD56. The modest quantity of NK cells in the blood available for functional analysis has been a limitation in studies of NK cell subpopulations. In the present study, epinephrine infusion was used to induce lymphocytosis before immunomagnetic methods were applied to isolate CD16+/-CD56+ and CD16+CD56- CD3- NK cells. These subpopulations were compared according to their proliferative and cytotoxic capabilities in 10 human immunodeficiency virus (HIV)-infected individuals and 5 healthy controls. The CD16+CD56- NK cell subgroup had a higher proliferative capacity, whereas the CD16+/-CD56+ NK cell subgroup was mainly cytotoxic, and unaffected by HIV serostatus. This study thus suggests that NK cell phenotypes more strongly predict NK cell function than HIV serostatus. This assertion should be considered when studying NK cell function in subjects with a deviating composition of NK cells.

KW - Adrenergic beta-Agonists

KW - Adult

KW - Antigens, CD56

KW - Biomarkers

KW - Cell Division

KW - Cell Movement

KW - Cytotoxicity, Immunologic

KW - Epinephrine

KW - Flow Cytometry

KW - HIV Infections

KW - HIV Seronegativity

KW - Humans

KW - Immunophenotyping

KW - Killer Cells, Natural

KW - Leukocyte Count

KW - Lymphocytosis

KW - Male

KW - Receptors, IgG

KW - Comparative Study

KW - Journal Article

KW - Research Support, Non-U.S. Gov't

M3 - Journal article

C2 - 11252817

VL - 108

SP - 831

EP - 837

JO - A P M I S. Acta Pathologica, Microbiologica et Immunologica Scandinavica

JF - A P M I S. Acta Pathologica, Microbiologica et Immunologica Scandinavica

SN - 0903-4641

IS - 12

ER -

ID: 180571552