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Biomedical subjects

J Lindenmann

Publications and source records attributed to J Lindenmann.

84 records · Page 5Linked to original sources
PubMed1969

Morphogenesis of influenza A virus in Ehrlich ascites tumor cells as revealed by thin-sectioning and freeze-etching.

The budding of a tumor-adapted strain of influenza A(0) virus at the surface of Ehrlich ascites tumor cells was studied by electron microscopy. Thin sections of budding sites showed the formation of a fuzzy coat on the outside of the cell membrane and simultaneously the apposition of a dark layer on the inner side. The continuity of cellular and viral membrane seemed to be preserved up to the point where the virion remained attached by only a thin stalk. Freeze-etching of virus budding sites yielded pictures in which a clear differentiation between the viral membrane and the host cell membrane was visible. The breaks across the fuzzy coat revealed striations corresponding to the "spikes" seen in negative contrast, whereas tangentially broken virus particles were best interpreted by assuming that splitting occurred midway between the two outer layers of the envelope.

Animals↗
PubMed1967

Viral oncolysis: increased immunogenicity of host cell antigen associated with influenza virus.

A2G mice could be solidly immunized against the Ehrlich ascites tumor by single intraperitoneal injections of homogenized and lyophilized tumor cells which had been infected with oncolytic strains of influenza A virus. Similar homogenates from noninfected tumor cells were not immunogenic, even when mixed with egg-grown virus. The immunizing principle in viral oncolysates could not be separated from the oncolytic virus by differential centrifugation or adsorption to and elution from red cells. It could be inhibited by antibody raised in rabbits against the egg-grown oncolytic virus. This reaction showed serologic specificity. Thus, the immunogenicity of an oncolysate produced with the WSA strain of neurotropic influenza virus could be inhibited by rabbit anti-WSA, but not by rabbit antibody to the TUR strain of fowl plague virus. Conversely, the immunogenicity of an oncolysate prepared with the TUR strain could be inhibited by rabbit anti-TUR, but not by anti-WSA. When mice were preimmunized (primed) with egg-grown WSA virus, their antitumor response to a later injection of WSA oncolysate was of the anamnestic type. Priming with egg-grown influenza B virus had no such effect. It was concluded that the immunogenicity of certain host cell components was greatly increased by incorporation into the makeup of the oncolytic virus.

Animals↗
PubMedDate not supplied

Homobodies: do they exist?

Within an immunological network consisting of interacting paratopes and idiotopes, three families of molecules can be postulated which bear a peculiarly close connection to any given epitope; the antibody, which carries paratopes which fit the epitope; the anti-idiotype, which carries paratopes fitting the idiotopes of the antibody; and the "homobody", which carries idiotopes to which the paratopes of the antibody fit. The homobody, called by Jerne the "internal image set", is a molecule which resembles the epitope, not like a mould resembles its cast, but like one cast resembles another cast made in the same mould. A distinction between homobody and anti-idiotype poses certain problems which are discussed in the light of a hypothetical experiment using avidin as the antigen.

Antibodies, Anti-Idiotypic↗