Murine Monoclonal Antibody 26 Raised Against Tetanus Toxoid Cross-Reacts with beta(2)-Glycoprotein I: Its Characteristics and Role in Molecular Mimicry
Само за регистроване кориснике
2009
Аутори
Inić-Kanada, AleksandraStojanović, Marijana
Živković, Irena
Kosec, Duško
Mićić, Mileva
Petrušić, Vladimir
Živančević-Simonović, Snežana
Dimitrijević, Ljiljana
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
Studies on experimental antiphospholipid syndrome (APS) models proved that molecular mimicry between plasma protein beta(2)-glycoprotein I (beta(2)GPI) and structure within micro-organisms or their products, might be a cause for experimental APS. Considering the heterogeneity of polyclonal antiphospholipid antibodies (aPLs), it is important to define the precise characteristics of pathogenic aPLs. To avoid the influence of polyclonality and to further analyse the connection between molecular mimicry and APS, we produced monoclonal antibodies (MAbs) against tetanus toxoid (TTd) and tested their reactivity against beta(2)GPI. In this report, we analysed the characteristics of MAb26 raised against TTd and cross-reactive with beta(2)GPI: its binding properties in various in vitro immunoassays, its specific interactions with surface epitopes expressed on apoptotic cells and its role in vivo. We have demonstrated that MAb26: (i) binds beta(2)GPI being immobilized on an appropriate surface: i...rradiated polystyrene plates, non-irradiated plates pre-coated with anionic phospholipids and polyvinylidene fluoride membrane; (ii) binds specifically to apoptotic but not to viable cells and the binding is beta(2)GPI-dependent; and (iii) induces a pathologic pregnancy outcome when passively injected into BALB/c mice. This study concluded that certain subpopulations of antibodies raised against TTd and cross-reactive with beta(2)GPI, because of the molecular mimicry mechanism, could have pathologic potential.
Кључне речи:
Antiphospholipid syndrome / fetal loss / molecular mimicry / tetanus toxoid / beta(2)-glycoprotein IИзвор:
American Journal of Reproductive Immunology, 2009, 61, 1, 39-51Издавач:
- Wiley, Hoboken
Финансирање / пројекти:
- Испитивање структуре и функције биолошки важних макромолекула у физиолошким и патолошким стањима (RS-MESTD-MPN2006-2010-142020)
DOI: 10.1111/j.1600-0897.2008.00660.x
ISSN: 1046-7408
PubMed: 19086991
WoS: 000261636900006
Scopus: 2-s2.0-57749199106
Институција/група
TorlakTY - JOUR AU - Inić-Kanada, Aleksandra AU - Stojanović, Marijana AU - Živković, Irena AU - Kosec, Duško AU - Mićić, Mileva AU - Petrušić, Vladimir AU - Živančević-Simonović, Snežana AU - Dimitrijević, Ljiljana PY - 2009 UR - http://intor.torlakinstitut.com/handle/123456789/283 AB - Studies on experimental antiphospholipid syndrome (APS) models proved that molecular mimicry between plasma protein beta(2)-glycoprotein I (beta(2)GPI) and structure within micro-organisms or their products, might be a cause for experimental APS. Considering the heterogeneity of polyclonal antiphospholipid antibodies (aPLs), it is important to define the precise characteristics of pathogenic aPLs. To avoid the influence of polyclonality and to further analyse the connection between molecular mimicry and APS, we produced monoclonal antibodies (MAbs) against tetanus toxoid (TTd) and tested their reactivity against beta(2)GPI. In this report, we analysed the characteristics of MAb26 raised against TTd and cross-reactive with beta(2)GPI: its binding properties in various in vitro immunoassays, its specific interactions with surface epitopes expressed on apoptotic cells and its role in vivo. We have demonstrated that MAb26: (i) binds beta(2)GPI being immobilized on an appropriate surface: irradiated polystyrene plates, non-irradiated plates pre-coated with anionic phospholipids and polyvinylidene fluoride membrane; (ii) binds specifically to apoptotic but not to viable cells and the binding is beta(2)GPI-dependent; and (iii) induces a pathologic pregnancy outcome when passively injected into BALB/c mice. This study concluded that certain subpopulations of antibodies raised against TTd and cross-reactive with beta(2)GPI, because of the molecular mimicry mechanism, could have pathologic potential. PB - Wiley, Hoboken T2 - American Journal of Reproductive Immunology T1 - Murine Monoclonal Antibody 26 Raised Against Tetanus Toxoid Cross-Reacts with beta(2)-Glycoprotein I: Its Characteristics and Role in Molecular Mimicry EP - 51 IS - 1 SP - 39 VL - 61 DO - 10.1111/j.1600-0897.2008.00660.x ER -
@article{ author = "Inić-Kanada, Aleksandra and Stojanović, Marijana and Živković, Irena and Kosec, Duško and Mićić, Mileva and Petrušić, Vladimir and Živančević-Simonović, Snežana and Dimitrijević, Ljiljana", year = "2009", abstract = "Studies on experimental antiphospholipid syndrome (APS) models proved that molecular mimicry between plasma protein beta(2)-glycoprotein I (beta(2)GPI) and structure within micro-organisms or their products, might be a cause for experimental APS. Considering the heterogeneity of polyclonal antiphospholipid antibodies (aPLs), it is important to define the precise characteristics of pathogenic aPLs. To avoid the influence of polyclonality and to further analyse the connection between molecular mimicry and APS, we produced monoclonal antibodies (MAbs) against tetanus toxoid (TTd) and tested their reactivity against beta(2)GPI. In this report, we analysed the characteristics of MAb26 raised against TTd and cross-reactive with beta(2)GPI: its binding properties in various in vitro immunoassays, its specific interactions with surface epitopes expressed on apoptotic cells and its role in vivo. We have demonstrated that MAb26: (i) binds beta(2)GPI being immobilized on an appropriate surface: irradiated polystyrene plates, non-irradiated plates pre-coated with anionic phospholipids and polyvinylidene fluoride membrane; (ii) binds specifically to apoptotic but not to viable cells and the binding is beta(2)GPI-dependent; and (iii) induces a pathologic pregnancy outcome when passively injected into BALB/c mice. This study concluded that certain subpopulations of antibodies raised against TTd and cross-reactive with beta(2)GPI, because of the molecular mimicry mechanism, could have pathologic potential.", publisher = "Wiley, Hoboken", journal = "American Journal of Reproductive Immunology", title = "Murine Monoclonal Antibody 26 Raised Against Tetanus Toxoid Cross-Reacts with beta(2)-Glycoprotein I: Its Characteristics and Role in Molecular Mimicry", pages = "51-39", number = "1", volume = "61", doi = "10.1111/j.1600-0897.2008.00660.x" }
Inić-Kanada, A., Stojanović, M., Živković, I., Kosec, D., Mićić, M., Petrušić, V., Živančević-Simonović, S.,& Dimitrijević, L.. (2009). Murine Monoclonal Antibody 26 Raised Against Tetanus Toxoid Cross-Reacts with beta(2)-Glycoprotein I: Its Characteristics and Role in Molecular Mimicry. in American Journal of Reproductive Immunology Wiley, Hoboken., 61(1), 39-51. https://doi.org/10.1111/j.1600-0897.2008.00660.x
Inić-Kanada A, Stojanović M, Živković I, Kosec D, Mićić M, Petrušić V, Živančević-Simonović S, Dimitrijević L. Murine Monoclonal Antibody 26 Raised Against Tetanus Toxoid Cross-Reacts with beta(2)-Glycoprotein I: Its Characteristics and Role in Molecular Mimicry. in American Journal of Reproductive Immunology. 2009;61(1):39-51. doi:10.1111/j.1600-0897.2008.00660.x .
Inić-Kanada, Aleksandra, Stojanović, Marijana, Živković, Irena, Kosec, Duško, Mićić, Mileva, Petrušić, Vladimir, Živančević-Simonović, Snežana, Dimitrijević, Ljiljana, "Murine Monoclonal Antibody 26 Raised Against Tetanus Toxoid Cross-Reacts with beta(2)-Glycoprotein I: Its Characteristics and Role in Molecular Mimicry" in American Journal of Reproductive Immunology, 61, no. 1 (2009):39-51, https://doi.org/10.1111/j.1600-0897.2008.00660.x . .