Roxithromycin inhibits chemokine-induced chemotaxis of Th1 and Th2 cells but regulatory T cells. 2009

Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
Department of Dermatology, Hamamatsu University School of Medicine, Hamamatsu, Japan. itoutai@hama-med.ac.jp

BACKGROUND Roxithromycin (RXM), a 14-member macrolide antibiotic, has a variety of bioregulatory functions such as anti-inflammatory effects, anti-oxidant effects, and modulation of immune responses. OBJECTIVE In this study, we analyzed the effect of RXM on chemokine-induced chemotaxis of Th1, Th2, and regulatory T (Treg) cells established from three normal human peripheral blood lymphocytes by the reported methods. RESULTS Incubation with 10 microM RXM for 18 h did not alter the expression profile of CXCR3 on Th1 cells and CCR4 on Th2 and Treg cells. However, upon RXM preincubation, the migration of Th1 cells to IP-10 and Th2 cells to TARC was partially suppressed, although RXM did not influence Treg cell migration. Erythromycin and clarithromycin at the same concentration did not exert such effects. F-actin polymerization and Ca(++) influx induced by IP-10 and TARC in Th1 and Th2 cells, respectively, was down-regulated by RXM pretreatment. CONCLUSIONS These results imply that RXM exhibits bioregulatory function by influencing chemotaxis of Th1 and Th2 cells while leaving Treg cell migration unaffected.

UI MeSH Term Description Entries
D007155 Immunologic Factors Biologically active substances whose activities affect or play a role in the functioning of the immune system. Biological Response Modifier,Biomodulator,Immune Factor,Immunological Factor,Immunomodulator,Immunomodulators,Biological Response Modifiers,Biomodulators,Factors, Immunologic,Immune Factors,Immunological Factors,Modifiers, Biological Response,Response Modifiers, Biological,Factor, Immune,Factor, Immunological,Factors, Immune,Factors, Immunological,Modifier, Biological Response,Response Modifier, Biological
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D002118 Calcium A basic element found in nearly all tissues. It is a member of the alkaline earth family of metals with the atomic symbol Ca, atomic number 20, and atomic weight 40. Calcium is the most abundant mineral in the body and combines with phosphorus to form calcium phosphate in the bones and teeth. It is essential for the normal functioning of nerves and muscles and plays a role in blood coagulation (as factor IV) and in many enzymatic processes. Coagulation Factor IV,Factor IV,Blood Coagulation Factor IV,Calcium-40,Calcium 40,Factor IV, Coagulation
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
D002633 Chemotaxis The movement of cells or organisms toward or away from a substance in response to its concentration gradient. Haptotaxis
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000199 Actins Filamentous proteins that are the main constituent of the thin filaments of muscle fibers. The filaments (known also as filamentous or F-actin) can be dissociated into their globular subunits; each subunit is composed of a single polypeptide 375 amino acids long. This is known as globular or G-actin. In conjunction with MYOSINS, actin is responsible for the contraction and relaxation of muscle. F-Actin,G-Actin,Actin,Isoactin,N-Actin,alpha-Actin,alpha-Isoactin,beta-Actin,gamma-Actin,F Actin,G Actin,N Actin,alpha Actin,alpha Isoactin,beta Actin,gamma Actin
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
February 2011, Journal of immunology (Baltimore, Md. : 1950),
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
July 1998, Journal of immunology (Baltimore, Md. : 1950),
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
August 2006, Cellular immunology,
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
March 1997, Science (New York, N.Y.),
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
January 2001, Scandinavian journal of immunology,
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
June 2010, European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology,
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
October 2019, Human immunology,
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
January 2000, Archivum immunologiae et therapiae experimentalis,
Taisuke Ito, and Natsuho Ito, and Hideo Hashizume, and Masahiro Takigawa
March 2003, Clinical & developmental immunology,
Copied contents to your clipboard!