TY - JOUR
T1 - Immune response and biochemistry of calves immunized with rMSP1a (Anaplasma marginale) using carbon nanotubes as carrier molecules
AU - Silvestre, Bruna Torres
AU - Da Silveira, Júlia Angélica Gonçalves
AU - Facury-Filho, Elias Jorge
AU - De Carvalho, Antônio Último
AU - Versiani, Alice Freitas
AU - Estevam, Letícia Gracielle Tôrres de Miranda
AU - Araújo, Márcio Sobreira Silva
AU - Martins-Filho, Olindo Assis
AU - Negrão-Corrêa, Deborah Aparecida
AU - Ribeiro, Múcio Flávio Barbosa
N1 - Funding Information:
The authors wish to thank UFMG (Universidade Federal de Minas Gerais), CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior), and Dr. Élida Mara Leite Rabelo and Dr. Flávio G. da Fonseca for their assistance with this study. This manuscript was reviewed by a professional scientific editor and by a native English-speaking copy editor to improve readability. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Vaccination against Anaplasma marginale has been considered an important control strategy for bovine anaplasmosis. Recently, mice immunized with rMSP1a linked to carbon nanotubes (MWNT) showed significant immune responses, generating a new possibility for use of an inactivated vaccine. The objective of this study was to investigate the cellular and humoral responses in calves immunized with MWNT+rMSP1a, associated with inactivated vaccine of A. marginale produced in vitro, and evaluate the toxic effects of the MWNT on renal and hepatic function. rMSP1a was covalently linked to MWNT. Inactivated vaccine (AmUFMG2) was produced by cultivating A. marginale in IDE8 cells. Twenty four Holstein calves were divided (four groups) and immunized subcutaneously with PBS and non-carboxylated MWNT (control, G1), AmUFMG2 (G2), MWNT+rMSP1a (G3), and AmUFMG2 with MWNT+rMSP1a (G4). Blood samples were collected for total leukocyte counts, biochemical profiling and evaluation of the cellular and humoral response. Immunization with MWNT+rMSP1a induced increase in the total number of leukocytes, NK cells, in the lymphocyte populations and higher levels of antibodies compared to calves immunized only with AmUFMG2. Furthermore, MWNT did not induce changes in the biochemical profile. These data indicate that MWNT+rMSP1a were able to induce the immune responses more efficiently than AmUFMG2 alone, without generating toxicity..
AB - Vaccination against Anaplasma marginale has been considered an important control strategy for bovine anaplasmosis. Recently, mice immunized with rMSP1a linked to carbon nanotubes (MWNT) showed significant immune responses, generating a new possibility for use of an inactivated vaccine. The objective of this study was to investigate the cellular and humoral responses in calves immunized with MWNT+rMSP1a, associated with inactivated vaccine of A. marginale produced in vitro, and evaluate the toxic effects of the MWNT on renal and hepatic function. rMSP1a was covalently linked to MWNT. Inactivated vaccine (AmUFMG2) was produced by cultivating A. marginale in IDE8 cells. Twenty four Holstein calves were divided (four groups) and immunized subcutaneously with PBS and non-carboxylated MWNT (control, G1), AmUFMG2 (G2), MWNT+rMSP1a (G3), and AmUFMG2 with MWNT+rMSP1a (G4). Blood samples were collected for total leukocyte counts, biochemical profiling and evaluation of the cellular and humoral response. Immunization with MWNT+rMSP1a induced increase in the total number of leukocytes, NK cells, in the lymphocyte populations and higher levels of antibodies compared to calves immunized only with AmUFMG2. Furthermore, MWNT did not induce changes in the biochemical profile. These data indicate that MWNT+rMSP1a were able to induce the immune responses more efficiently than AmUFMG2 alone, without generating toxicity..
KW - Anaplasma marginale
KW - Carbon nanotubes
KW - Inactivate vaccine
KW - MSP1a
UR - http://www.scopus.com/inward/record.url?scp=85049047017&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85049047017&partnerID=8YFLogxK
U2 - 10.1590/S1984-296120180029
DO - 10.1590/S1984-296120180029
M3 - Article
C2 - 29846449
AN - SCOPUS:85049047017
SN - 0103-846X
VL - 27
SP - 191
EP - 202
JO - Revista Brasileira de Parasitologia Veterinaria
JF - Revista Brasileira de Parasitologia Veterinaria
IS - 2
ER -