Abstract
The cellular responses to intraperitoneal inoculation of infective (L3) or non-infective (L2) larvae of Nippostrongylus brasiliensis were studied in unprimed rats. Peritoneal macrophages adhered to the larvae immediately after inoculation and the coated larvae became attached to the omentum. As additional inflammatory cells, appearing in the peritoneal exudate, adhered to the larvae, nodules were formed which with time organized into granulomas.
The initial response was not specific and consisted of an intense neutrophilia which developed in all rats a few hours after inoculation and lasted 24 hours. Thereafter the cellular responses were distinctly different in the case of each larval stage. In rats receiving L3 larvae an intense eosinophilia in the peritoneal exudate began to develop 7 days after inoculation, and islands of numerous pyroninophilic blast- and plasma cells were present at the periphery of the granuloma. The L3 larvae survived in the granulomas for 7–10 days.
The granulomas formed around the L2 larvae consisted mainly of macrophages; the number of eosinophils did not rise above normal and there were no pyroninophilic cells. The L2 larvae survived in the granuloma for 3 days. In control rats, in which an intestinal infection was established by subcutaneous administration of larvae, no changes were detected in the cellular composition of the peritoneal exudate.
The significance of these responses is discussed in relation to recent reports about the cellular composition of antigenic and non-antigenic granulomas.
Full text
PDF












Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Athanassiades T. J., Speirs R. S. Granuloma induction in the peritoneal cavity. A model for the study of inflammation and plasmacytopoiesis in nonlymphatic organs. J Reticuloendothel Soc. 1972 Jan;11(1):60–76. [PubMed] [Google Scholar]
- Basten A., Beeson P. B. Mechanism of eosinophilia. II. Role of the lymphocyte. J Exp Med. 1970 Jun 1;131(6):1288–1305. doi: 10.1084/jem.131.6.1288. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Basten A., Boyer M. H., Beeson P. B. Mechanism of eosinophilia. I. Factors affecting the eosinophil response of rats to Trichinella spiralis. J Exp Med. 1970 Jun 1;131(6):1271–1287. doi: 10.1084/jem.131.6.1271. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crandall C. A., Crandall R. B., Arean V. M. Increased resistance in mice to larval Ascaris suum infection induced by Nippostrongylus brasiliensis. J Parasitol. 1967 Feb;53(1):214–215. [PubMed] [Google Scholar]
- Jackson G. J., Bradbury P. C. Cuticular fine structure and molting of Neoaplectana glaseri (Nematoda), after prolonged contact with rat peritoneal exudate. J Parasitol. 1970 Feb;56(1):108–115. [PubMed] [Google Scholar]
- Jeska E. L. Mouse peritoneal exudate cell reactions to parasitic worms. I. Cell adhesion reactions. Immunology. 1969 Jun;16(6):761–771. [PMC free article] [PubMed] [Google Scholar]
- KEELING J. E. The effects of ultra-violet radiation on Nippostrongylus muris. I. Irradiation of infective larvae: lethal and sublethal effects. Ann Trop Med Parasitol. 1960 Jun;54:182–191. doi: 10.1080/00034983.1960.11685974. [DOI] [PubMed] [Google Scholar]
- Ogilvie B. M., Jones V. E. Parasitological review. Nippostrongylus brasiliensis: a review of immunity and host-parasite relationship in the rat. Exp Parasitol. 1971 Feb;29(1):138–177. doi: 10.1016/0014-4894(71)90021-x. [DOI] [PubMed] [Google Scholar]
- PADAWER J., GORDON A. S. Cellular elements in the peritoneal fluid of some mammals. Anat Rec. 1956 Feb;124(2):209–222. doi: 10.1002/ar.1091240206. [DOI] [PubMed] [Google Scholar]
- SOULSBY E. J. THE NATURE AND ORIGIN OF THE FUNCTIONAL ANTIGENS IN HELMINTH INFECTIONS. Ann N Y Acad Sci. 1963 Dec 30;113:492–509. doi: 10.1111/j.1749-6632.1963.tb40686.x. [DOI] [PubMed] [Google Scholar]
- Schneerson-Porat S., Shahar A., Aronson M. Formation of histiocyte rings in response to Cryptococcus neoformans infection. J Reticuloendothel Soc. 1965 Sep;2(3):249–255. [PubMed] [Google Scholar]
- Shahar A., Kletter Y., Aronson M. Granuloma formation in cryptococcosis. Isr J Med Sci. 1969 Nov-Dec;5(6):1164–1172. [PubMed] [Google Scholar]
- Simaren J. O. Host response and biologic differentiation of Nippostrongylus brasiliensis. Ann Parasitol Hum Comp. 1970 Jul-Aug;45(4):421–429. doi: 10.1051/parasite/1970454421. [DOI] [PubMed] [Google Scholar]
- Slonecker C. E. The cellular composition of an acute inflammatory exudate in rats. J Reticuloendothel Soc. 1971 Sep;10(3):269–282. [PubMed] [Google Scholar]








