Characterization of neutralizing monoclonal antibodies directed against tetanus toxin fragment C. (January 2014)
- Record Type:
- Journal Article
- Title:
- Characterization of neutralizing monoclonal antibodies directed against tetanus toxin fragment C. (January 2014)
- Main Title:
- Characterization of neutralizing monoclonal antibodies directed against tetanus toxin fragment C
- Authors:
- Yousefi, Mehdi
Tahmasebi, Fathollah
Younesi, Vahid
Razavi, Alireza
Khoshnoodi, Jalal
Bayat, Ali Ahmad
Abbasi, Ebrahim
Rabbani, Hodjatallah
Jeddi-Tehrani, Mahmood
Shokri, Fazel - Abstract:
- <abstract> <title>Abstract</title> <p> <italic>Clostridium tetani</italic> causes a life-threatening infectious disease by production of tetanus neurotoxin (TeNT), a 150 kDa molecule composed of light (LC) and heavy chain (HC) polypeptides. The TeNT HC contains an N-terminal domain critical for LC translocation and a C-terminal toxin receptor-binding domain known as fragment C. Despite extensive investigations on epitope specificity of anti-TeNT antibodies, the immunodominant neutralizing epitopes of the toxin are poorly defined. This study describes the generation and characterization of four monoclonal antibodies (MAb) specific for TeNT. The characteristics of each MAb were explored in terms of isotype, specificity, affinity, and immuno-globulin heavy chain variable region (IGHV) gene usage using ELISA, Western blotting, and sequencing techniques. The toxin neutralizing activity of the MAbs was also investigated using the <italic>in vitro</italic> GT1b neutralizing assay. The data demonstrated that all MAbs bind to tetanus toxin and toxoid. Sub-fragments binding analysis showed that two MAbs react with fragment C, one with both fragment C and LC, and one with LC. Only the two fragment C-specific MAbs were able to neutralize the toxin. Sequencing of the expressed VH and VL genes revealed rearrangements of various VH and VL gene segments in all hybridoma clones. Clonality of the hybridomas was also confirmed by a competition assay that showed recognition of distinct epitopes<abstract> <title>Abstract</title> <p> <italic>Clostridium tetani</italic> causes a life-threatening infectious disease by production of tetanus neurotoxin (TeNT), a 150 kDa molecule composed of light (LC) and heavy chain (HC) polypeptides. The TeNT HC contains an N-terminal domain critical for LC translocation and a C-terminal toxin receptor-binding domain known as fragment C. Despite extensive investigations on epitope specificity of anti-TeNT antibodies, the immunodominant neutralizing epitopes of the toxin are poorly defined. This study describes the generation and characterization of four monoclonal antibodies (MAb) specific for TeNT. The characteristics of each MAb were explored in terms of isotype, specificity, affinity, and immuno-globulin heavy chain variable region (IGHV) gene usage using ELISA, Western blotting, and sequencing techniques. The toxin neutralizing activity of the MAbs was also investigated using the <italic>in vitro</italic> GT1b neutralizing assay. The data demonstrated that all MAbs bind to tetanus toxin and toxoid. Sub-fragments binding analysis showed that two MAbs react with fragment C, one with both fragment C and LC, and one with LC. Only the two fragment C-specific MAbs were able to neutralize the toxin. Sequencing of the expressed VH and VL genes revealed rearrangements of various VH and VL gene segments in all hybridoma clones. Clonality of the hybridomas was also confirmed by a competition assay that showed recognition of distinct epitopes by these MAbs. The results suggest the importance of TeNT fragment C in terms of immunogenicity and toxin neutralization activity.</p> </abstract> … (more)
- Is Part Of:
- Journal of immunotoxicology. Volume 11:Number 1(2014)
- Journal:
- Journal of immunotoxicology
- Issue:
- Volume 11:Number 1(2014)
- Issue Display:
- Volume 11, Issue 1 (2014)
- Year:
- 2014
- Volume:
- 11
- Issue:
- 1
- Issue Sort Value:
- 2014-0011-0001-0000
- Page Start:
- 28
- Page End:
- 34
- Publication Date:
- 2014-01
- Subjects:
- Immunotoxicology -- Periodicals
Poisons -- Immunology -- Periodicals
Environmental health -- Periodicals
616.97 - Journal URLs:
- http://informahealthcare.com ↗
- DOI:
- 10.3109/1547691X.2013.763872 ↗
- Languages:
- English
- ISSNs:
- 1547-691X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5005.043000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3369.xml