The restoration of impaired macrophage functions using as immunomodulator the Corynebacterium granulosum-derived P40 fraction

Many microorganisms and compounds of microbial origin exhibit immunomodulatory activities and have been extensively used in immunotherapy of experimental animal tumors and in patients with neoplasia. In this paper we describe the effect of the C. granulosum-derived P40 fraction on the growth and met...

Full description

Saved in:
Bibliographic Details
Published inImmunopharmacology Vol. 10; no. 1; p. 27
Main Authors Mastroeni, P, Bizzini, B, Bonina, L, Iannello, D, Merendino, R A, Delfino, D, Berlinghieri, M C, Leonardi, M S, Arena, A, Liberto, M C
Format Journal Article
LanguageEnglish
Published Netherlands 01.01.1985
Subjects
Online AccessGet more information

Cover

Loading…
More Information
Summary:Many microorganisms and compounds of microbial origin exhibit immunomodulatory activities and have been extensively used in immunotherapy of experimental animal tumors and in patients with neoplasia. In this paper we describe the effect of the C. granulosum-derived P40 fraction on the growth and metastatization of the transplantable epithelioma T8 of Guèrin. Moreover, we evaluated the effect of P40 treatment on several depressed macrophage functions of tumor-bearing rats. In particular, the phagocytic and chemotactic activities of such cells were studied, as well as the antiviral intrinsic and extrinsic activities against HSV-1 and the anti-Toxoplasma gondii activity. All these functions were depressed in untreated tumor-bearing rats. Administration of a single intravenous injection of P40 fraction led to the restoration of all depressed macrophage activities to normal values. In particular, the possibility of restoring the antimicrobial activity of macrophages from tumor-bearing rats by treatment with this immunomodulator is of great concern when one considers the increasing incidence of opportunistic infections in immunocompromised hosts. Results are discussed in terms of both the possible mechanism of action of P40 and of its possible target cells.
ISSN:0162-3109
DOI:10.1016/0162-3109(85)90056-6