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Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa).
The immunogenicity of a soluble fraction containing Gross-virus-associated cell-surface antigen (GCSAa) obtained from (C58NT)D lymphoma cells either by detergent (NP40) solubilization or by 3M KCl extraction, was studied in syngeneic W/Fu rats. Rats immunized by 2 s.c. injections of soluble antigen...
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1980
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010207/ https://www.ncbi.nlm.nih.gov/pubmed/7370163 |
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author | Gerlier, D. Sakai, F. Doré, J. F. |
author_facet | Gerlier, D. Sakai, F. Doré, J. F. |
author_sort | Gerlier, D. |
collection | PubMed |
description | The immunogenicity of a soluble fraction containing Gross-virus-associated cell-surface antigen (GCSAa) obtained from (C58NT)D lymphoma cells either by detergent (NP40) solubilization or by 3M KCl extraction, was studied in syngeneic W/Fu rats. Rats immunized by 2 s.c. injections of soluble antigen or soluble antigen mixed with empty liposomes and emulsified in complete Freund's adjuvant (CFA) failed to produce significant levels of cytotoxic antibodies to GCSAa. On the other hand, rats similarly immunized by negatively charged liposomes containing NP40-solubilized GCSAa, and emulsified in CFA, developed high and persistent levels of cytotoxic antibodies, and their response could even mimic that induced by viable (C58NT)D cells. A similar response could also be obtained in rats immunized with liposome-associated NP40-solubilized GCSAa, but without CFA. Rats immunized by comparable amounts of liposome-assocated 3M KCl-extracted GCSAa developed only low levels of cytotoxic antibodies, and their response was of shorter duration. These results strongly suggest that inclusion into liposomes of a solubilized proteic tumour-associated cell-surface antigen can provide an immunogen as potent as viable tumour cells in inducing an antibody response, and that the solubilization method may be critical. |
format | Text |
id | pubmed-2010207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1980 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20102072009-09-10 Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa). Gerlier, D. Sakai, F. Doré, J. F. Br J Cancer Research Article The immunogenicity of a soluble fraction containing Gross-virus-associated cell-surface antigen (GCSAa) obtained from (C58NT)D lymphoma cells either by detergent (NP40) solubilization or by 3M KCl extraction, was studied in syngeneic W/Fu rats. Rats immunized by 2 s.c. injections of soluble antigen or soluble antigen mixed with empty liposomes and emulsified in complete Freund's adjuvant (CFA) failed to produce significant levels of cytotoxic antibodies to GCSAa. On the other hand, rats similarly immunized by negatively charged liposomes containing NP40-solubilized GCSAa, and emulsified in CFA, developed high and persistent levels of cytotoxic antibodies, and their response could even mimic that induced by viable (C58NT)D cells. A similar response could also be obtained in rats immunized with liposome-associated NP40-solubilized GCSAa, but without CFA. Rats immunized by comparable amounts of liposome-assocated 3M KCl-extracted GCSAa developed only low levels of cytotoxic antibodies, and their response was of shorter duration. These results strongly suggest that inclusion into liposomes of a solubilized proteic tumour-associated cell-surface antigen can provide an immunogen as potent as viable tumour cells in inducing an antibody response, and that the solubilization method may be critical. Nature Publishing Group 1980-02 /pmc/articles/PMC2010207/ /pubmed/7370163 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Gerlier, D. Sakai, F. Doré, J. F. Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa). |
title | Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa). |
title_full | Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa). |
title_fullStr | Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa). |
title_full_unstemmed | Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa). |
title_short | Induction of antibody response to liposome-associated Gross-virus cell-surface antigen (GCSAa). |
title_sort | induction of antibody response to liposome-associated gross-virus cell-surface antigen (gcsaa). |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010207/ https://www.ncbi.nlm.nih.gov/pubmed/7370163 |
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