Induction of Th1-type cytokines by lipoteichoic acid-related preparation isolated from OK-432, a penicillin-killed streptococcal agent

Immunopharmacology. 2000 Sep;49(3):363-76. doi: 10.1016/s0162-3109(00)00252-6.

Abstract

We have isolated the lipoteichoic acid (LTA)-related molecule (OK-PSA) from OK-432, a streptococcal preparation, by an affinity chromatography on CNBr-activated Sepharose 4B-bound TS-2 monoclonal antibody (mAb) that neutralizes interferon (IFN)-gamma-inducing activity of OK-432. In in vitro experiments using human peripheral blood mononuclear cells (PBMC), OK-PSA induced IFN-gamma, interleukin (IL)-2, IL-12, IL-18, tumor necrosis factor (TNF)-alpha and TNF-beta that are generally called "Th1-type cytokines" both in protein and in mRNA levels. Furthermore, the neutralizing test using cytokine-specific antibodies demonstrated that IL-18 plays a most significant role for IFN-gamma- and killer cell-inducing ability of OK-PSA among the other cytokines tested. These findings clearly indicated that OK-PSA, an LTA-related molecule, is a main effective component of OK-432, and is a potent inducer of Th1-type cytokines by T cell and natural killer (NK) cell activation mediated by monocytes-derived IL-18, and that it may be a useful immunotherapeutic agent for the patients with malignancies better than original OK-432.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Bacterial*
  • Bacterial Outer Membrane Proteins*
  • Bacterial Proteins / isolation & purification
  • Bacterial Proteins / pharmacology
  • Carrier Proteins / isolation & purification
  • Carrier Proteins / pharmacology
  • Caspase 1 / metabolism
  • Caspase 1 / physiology
  • Cytokines / biosynthesis*
  • Cytokines / genetics
  • Cytotoxicity, Immunologic / drug effects
  • Enzyme Activation / drug effects
  • Enzyme Activation / immunology
  • Humans
  • Interferon-gamma / biosynthesis
  • Interleukin-10 / biosynthesis
  • Interleukin-18 / metabolism
  • K562 Cells
  • Killer Cells, Natural / drug effects
  • Killer Cells, Natural / immunology
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Lipopolysaccharides / pharmacology*
  • Lymphocyte Activation / drug effects
  • Mice
  • Mice, Inbred BALB C
  • Penicillins / pharmacology*
  • Picibanil / pharmacology*
  • RNA, Messenger / biosynthesis
  • Streptococcus pyogenes / immunology*
  • Teichoic Acids / pharmacology*
  • Th1 Cells / drug effects
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism

Substances

  • Antigens, Bacterial
  • Bacterial Outer Membrane Proteins
  • Bacterial Proteins
  • Carrier Proteins
  • Cytokines
  • Interleukin-18
  • Lipopolysaccharides
  • Penicillins
  • RNA, Messenger
  • Teichoic Acids
  • streptococcal M protein
  • Interleukin-10
  • Picibanil
  • lipoteichoic acid
  • Interferon-gamma
  • Caspase 1