Literature DB >> 6944271

The antibody-independent cytotoxic activity of normal circulating human leucocytes. II. Failure to demonstrate effector cell-target cell interaction and target cell specificity of the circulating cytotoxic-enhancing factor.

M Richter, D Banerjee, S Sklar.   

Abstract

The naturally-occurring antibody-independent cellular cytotoxic activity (NOCC) of normal circulating human monocytes and neutrophils was investigated employing a number of erythrocytes and the K-562 cell line as target cells simultaneously. The identity of the effector cell(s) was shown to be dependent upon or be a function of the type of target cell selected for the assay system. A number of erythrocyte targets (rabbit, horse, sheep and ox erythrocytes) were lysed to varying degrees by neutrophils and monocytes and not by lymphocytes. Irrespective of the red blood cell (RBC) target, the effector monocyte invariably possessed receptors for both C'3 and the Fc of IgG. In contrast, the cytotoxic cells using the K-562 target cell were lymphocytes. Monocytes and neutrophils were inactive. The cytotoxic-enhancing activity in normal human serum exhibits specific and non-specific properties which suggests that more than one factor is involved. With respect to the monocyte cytotoxic cells, only the rabbit erythrocytes could totally absorb the serum factor in a specific fashion. Absorption of the serum with horse, sheep or ox erythrocytes resulted in a significant loss of potentiating activity with respect to all of the erythrocyte targets but a more marked loss of activity using the absorbing erythrocytes as targets. With respect to the polymorphonuclear leucocyte effector cells, only the rabbit RBC were capable of specifically absorbing out the cytotoxic-enhancing factor present in the normal human serum. Absorption of the serum with sheep, horse or ox RBC resulted in total cross-absorption of the enhancing factor. Chicken and human RBC, which do not serve as targets for the NOCC assay, could not absorb out the cytotoxic-enhancing factor with respect to any of the target erythrocytes. The composition of the soluble serum factor(s) is under current investigation but it is not an immunoglobulin since pure serum albumin can substitute for normal serum in the NOCC assay. The mechanism of erythrocyte lysis by the cytotoxic monocyte was investigated. Mononuclear cells were incubated with target cell monolayers and with target cells under optimal rosetting conditions. No interaction between the effector and target cells could be detected. The monocytes did not adhere to the target cell monolayer nor did they form rosettes with the target cells. Thus, the results fail to corroborate or support the assumption that the cytotoxic activity of the monocyte is dependent upon conventionally-detectable receptors. Erythrophagocytosis was not observed to any significant degree under the assay conditions used. Therefore, the nature of the interaction between the cytotoxic monocyte and the erythroid target cell which results in lysis of the target cell remains to be elucidated.

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Year:  1981        PMID: 6944271      PMCID: PMC1555109     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  32 in total

1.  The nonselective cytotoxic cell (N cell).

Authors:  M Kiuchi; M Takasugi
Journal:  J Natl Cancer Inst       Date:  1976-03       Impact factor: 13.506

2.  Cytotoxicity of alveolar macrophages for virus-infected cells.

Authors:  E J Stott; M Probert; L H Thomas
Journal:  Nature       Date:  1975-06-26       Impact factor: 49.962

3.  Cytotoxity of non-T versus T-lymphocytes from melanoma patients and healthy donors on short- and long-term cultured melanoma cells,.

Authors:  J E de Vries; S Cornain; P Rumke
Journal:  Int J Cancer       Date:  1974-10-15       Impact factor: 7.396

4.  Cells involved in cell-mediated and transplantation immunity in the rabbit. 8. The killer cell activity of the lymphocytes in the gastrointestine-associated lymphoid organs of the normal unsensitized adult rabbit.

Authors:  Y Behelak; M Richter
Journal:  Transplantation       Date:  1974-09       Impact factor: 4.939

5.  Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic and allogeneic tumors. II. Characterization of effector cells.

Authors:  R B Herberman; M E Nunn; H T Holden; D H Lavrin
Journal:  Int J Cancer       Date:  1975-08-15       Impact factor: 7.396

6.  "Natural" killer cells in the mouse. II. Cytotoxic cells with specificity for mouse Moloney leukemia cells. Characteristics of the killer cell.

Authors:  R Kiessling; E Klein; H Pross; H Wigzell
Journal:  Eur J Immunol       Date:  1975-02       Impact factor: 5.532

7.  Cytotoxic lymphocytes from normal donors. A functional marker of human non-T lymphocytes.

Authors:  H F Pross; M Jondal
Journal:  Clin Exp Immunol       Date:  1975-08       Impact factor: 4.330

8.  Specificity of cell-mediated cytotoxicity against human melanoma lines: evidence for "non-specific" killing by activated T-cells.

Authors:  P Hersey; A Edwards; J Edwards; E Adams; G W Milton; D S Nelson
Journal:  Int J Cancer       Date:  1975-07-15       Impact factor: 7.396

9.  Surface markers on human b and t lymphocytes. VI. Cytotoxicity against cell lines as a functional marker for lymphocyte subpopulations.

Authors:  M Jondal; H Pross
Journal:  Int J Cancer       Date:  1975-04-15       Impact factor: 7.396

10.  Killer cells: a functional comparison between natural, immune T-cell and antibody-dependent in vitro systems.

Authors:  R Kiessling; G Petranyi; K Kärre; M Jondal; D Tracey; H Wigzell
Journal:  J Exp Med       Date:  1976-04-01       Impact factor: 14.307

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