In vitro immunization approach to generate specific murine monoclonal IgG antibodies
- Generating a monoclonal antibody to date is a time intense process that requires immunization of laboratory animals. The transfer of the humoral immune response into in vitro settings enables a shortening of this process and circumvents the necessity of in vivo immunization. However, to orchestrate the complex interplay of dendritic cells, T and B lymphocytes in vitro is very challenging. We therefore aimed for a simplified approach focusing on the protagonist of antibody production: the B lymphocyte. We activated purified murine B lymphocytes alone in vitro by using combinations of antigen and stimuli. We were able to induce a specific antibody response within ten days of culture against a viral coat protein as model antigen. Antibodies were of both IgM and IgG subclass. The stimulated B lymphocytes were transformed into permanently antibody-producing hybridomas by cell fusion technology. We furthermore used this method to induce a specific antibody response against L. pneumophila in vitro. We thus established a useful and effectiveGenerating a monoclonal antibody to date is a time intense process that requires immunization of laboratory animals. The transfer of the humoral immune response into in vitro settings enables a shortening of this process and circumvents the necessity of in vivo immunization. However, to orchestrate the complex interplay of dendritic cells, T and B lymphocytes in vitro is very challenging. We therefore aimed for a simplified approach focusing on the protagonist of antibody production: the B lymphocyte. We activated purified murine B lymphocytes alone in vitro by using combinations of antigen and stimuli. We were able to induce a specific antibody response within ten days of culture against a viral coat protein as model antigen. Antibodies were of both IgM and IgG subclass. The stimulated B lymphocytes were transformed into permanently antibody-producing hybridomas by cell fusion technology. We furthermore used this method to induce a specific antibody response against L. pneumophila in vitro. We thus established a useful and effective in vitro protocol to generate monoclonal antibodies. By overcoming the necessity of in vivo immunization this protocol may be the first step towards a universal strategy to generate antibodies from various species.…
Verfasserangaben: | Sophia MichelchenORCiDGND, Burkhard MicheelORCiD, Katja HanackORCiDGND |
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DOI: | https://doi.org/10.1016/j.jim.2021.113149 |
ISSN: | 0022-1759 |
ISSN: | 1872-7905 |
Pubmed ID: | https://pubmed.ncbi.nlm.nih.gov/34560072 |
Titel des übergeordneten Werks (Englisch): | Journal of immunological methods : JIM |
Verlag: | Elsevier |
Verlagsort: | Amsterdam |
Publikationstyp: | Wissenschaftlicher Artikel |
Sprache: | Englisch |
Datum der Erstveröffentlichung: | 01.12.2021 |
Erscheinungsjahr: | 2021 |
Datum der Freischaltung: | 24.03.2023 |
Freies Schlagwort / Tag: | B cell activation; Hybridoma technology; In vitro immunization; Monoclonal antibody |
Band: | 499 |
Aufsatznummer: | 113149 |
Seitenanzahl: | 8 |
Fördernde Institution: | German Federal Ministry of Education and ResearchFederal Ministry of Education & Research (BMBF) [03IPT7030X] |
Organisationseinheiten: | Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie |
DDC-Klassifikation: | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
Peer Review: | Referiert |