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- Publisher Website: 10.1111/j.1699-0463.1991.tb05172.x
- Scopus: eid_2-s2.0-0025729660
- PMID: 1904250
- WOS: WOS:A1991FQ49800006
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Article: The effects of blockade of interleukin 2 receptors and interleukin 4 receptors on cytokine production
Title | The effects of blockade of interleukin 2 receptors and interleukin 4 receptors on cytokine production |
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Authors | |
Keywords | interleukin 2 interleukin 4 interleukin 6 peripheral blood lymphocytes receptor blockade |
Issue Date | 1991 |
Publisher | Wiley-Blackwell Publishing, Inc. The Journal's web site is located at http://www.blackwellpublishing.com/journals/APMIS |
Citation | Apmis, 1991, v. 99 n. 5, p. 434-442 How to Cite? |
Abstract | The understanding of the regulation of cytokine production and T-cell proliferation by other cytokines is far from complete. We have examined the supernatant concentration of different cytokines in cultured peripheral blood lymphocytes (PBL) incubated with monoclonal antibodies against the interleukin-2 receptor (IL-2R) or interleukin-4 receptor (IL-4R) complex in order to analyse the importance of these receptors in the production of other cytokines. The PBL cultures were stimulated with phytohaemagglutinin and phorbol myristate acetate. The addition of anti-Tac to PBL cultures resulted in increased free IL-2 due to blockade of IL-2R. MR6 (a monoclonal antibody against IL-4R) did not affect the supernatant concentration of IL-2 in cultured PBL. Blockade of IL-2R or IL-4R both resulted in increased IL-4 in supernatant. The increase in supernatant concentration of IL-4 in PBL cultured with MR6 was due to a direct interaction with the IL-4R complex but the increase in lL-4 with anti-Tac was due to the accumulation of free IL-4 as an effective blockade of IL-2R prevented the full expression of IL-4R. Neither anti-Tac nor MR6 affected the IL-6 production by activated PBL, suggesting the existence of an IL-2- and IL-4-independent pathway. Blockade of IL-2R or IL-4R both resulted in a reduction of interferon-gamma (IFN-gamma) production, indicating that both endogenously generated IL-2 and IL-4 are important mediators of IFN-gamma induction in PBL cultures stimulated with T-cell mitogens. |
Persistent Identifier | http://hdl.handle.net/10722/161856 |
ISSN | 2023 Impact Factor: 2.2 2023 SCImago Journal Rankings: 0.687 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lai, KN | en_HK |
dc.contributor.author | Leung, JCK | en_HK |
dc.contributor.author | Li, PKT | en_HK |
dc.contributor.author | Larche, M | en_HK |
dc.contributor.author | Ritter, MA | en_HK |
dc.date.accessioned | 2012-09-05T05:15:33Z | - |
dc.date.available | 2012-09-05T05:15:33Z | - |
dc.date.issued | 1991 | en_HK |
dc.identifier.citation | Apmis, 1991, v. 99 n. 5, p. 434-442 | en_HK |
dc.identifier.issn | 0903-4641 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/161856 | - |
dc.description.abstract | The understanding of the regulation of cytokine production and T-cell proliferation by other cytokines is far from complete. We have examined the supernatant concentration of different cytokines in cultured peripheral blood lymphocytes (PBL) incubated with monoclonal antibodies against the interleukin-2 receptor (IL-2R) or interleukin-4 receptor (IL-4R) complex in order to analyse the importance of these receptors in the production of other cytokines. The PBL cultures were stimulated with phytohaemagglutinin and phorbol myristate acetate. The addition of anti-Tac to PBL cultures resulted in increased free IL-2 due to blockade of IL-2R. MR6 (a monoclonal antibody against IL-4R) did not affect the supernatant concentration of IL-2 in cultured PBL. Blockade of IL-2R or IL-4R both resulted in increased IL-4 in supernatant. The increase in supernatant concentration of IL-4 in PBL cultured with MR6 was due to a direct interaction with the IL-4R complex but the increase in lL-4 with anti-Tac was due to the accumulation of free IL-4 as an effective blockade of IL-2R prevented the full expression of IL-4R. Neither anti-Tac nor MR6 affected the IL-6 production by activated PBL, suggesting the existence of an IL-2- and IL-4-independent pathway. Blockade of IL-2R or IL-4R both resulted in a reduction of interferon-gamma (IFN-gamma) production, indicating that both endogenously generated IL-2 and IL-4 are important mediators of IFN-gamma induction in PBL cultures stimulated with T-cell mitogens. | en_HK |
dc.language | eng | en_US |
dc.publisher | Wiley-Blackwell Publishing, Inc. The Journal's web site is located at http://www.blackwellpublishing.com/journals/APMIS | en_HK |
dc.relation.ispartof | APMIS | en_HK |
dc.subject | interleukin 2 | en_HK |
dc.subject | interleukin 4 | en_HK |
dc.subject | interleukin 6 | en_HK |
dc.subject | peripheral blood lymphocytes | en_HK |
dc.subject | receptor blockade | en_HK |
dc.subject.mesh | Antibodies, Monoclonal - Diagnostic Use | en_US |
dc.subject.mesh | Antigens, Cd - Analysis | en_US |
dc.subject.mesh | Cells, Cultured | en_US |
dc.subject.mesh | Culture Techniques - Methods | en_US |
dc.subject.mesh | Cytokines - Biosynthesis | en_US |
dc.subject.mesh | Dna Replication | en_US |
dc.subject.mesh | Enzyme-Linked Immunosorbent Assay | en_US |
dc.subject.mesh | Fluorescent Antibody Technique | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Interferon-Gamma - Analysis - Biosynthesis | en_US |
dc.subject.mesh | Interleukin-2 - Analysis - Biosynthesis | en_US |
dc.subject.mesh | Interleukin-4 - Analysis - Biosynthesis | en_US |
dc.subject.mesh | Kinetics | en_US |
dc.subject.mesh | Lymphocyte Activation | en_US |
dc.subject.mesh | Lymphocytes - Drug Effects - Immunology | en_US |
dc.subject.mesh | Receptors, Interleukin-2 - Analysis - Immunology - Physiology | en_US |
dc.subject.mesh | Receptors, Interleukin-4 | en_US |
dc.subject.mesh | Receptors, Mitogen - Immunology - Physiology | en_US |
dc.title | The effects of blockade of interleukin 2 receptors and interleukin 4 receptors on cytokine production | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Lai, KN: knlai@hku.hk | en_HK |
dc.identifier.email | Leung, JCK: jckleung@hku.hk | en_HK |
dc.identifier.authority | Lai, KN=rp00324 | en_HK |
dc.identifier.authority | Leung, JCK=rp00448 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1111/j.1699-0463.1991.tb05172.x | - |
dc.identifier.pmid | 1904250 | - |
dc.identifier.scopus | eid_2-s2.0-0025729660 | en_HK |
dc.identifier.volume | 99 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 434 | en_HK |
dc.identifier.epage | 442 | en_HK |
dc.identifier.isi | WOS:A1991FQ49800006 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Lai, KN=7402135706 | en_HK |
dc.identifier.scopusauthorid | Leung, JCK=7202180349 | en_HK |
dc.identifier.scopusauthorid | Li, PKT=25928016800 | en_HK |
dc.identifier.scopusauthorid | Larche, M=7006394560 | en_HK |
dc.identifier.scopusauthorid | Ritter, MA=7402696170 | en_HK |
dc.identifier.issnl | 0903-4641 | - |