Literature DB >> 10652120

Helper T cell and antibody responses to infection of CBA mice with Babesia microti.

D Chen1, D B Copeman, J Burnell, G W Hutchinson.   

Abstract

Helper T cell cytokine and antibody responses were investigated in mice after infection with Babesia microti (King strain). Infection of CBA mice with 106 parasitized erythrocytes resulted in the development of a transitory high parasitaemia which peaked 14 days post infection (DPI), and was resolved at 24 DPI. Th1 responses were activated predominately during the acute phase (6-18 DPI) whereas Th2 responses predominated during the recovery phase (14-28 DPI) as detected by the reverse transcriptase polymerase chain reaction. Increased expression of Th1 cytokines was first detected at 6 DPI (IL-2) and 8 DPI (IFN-gamma) and their peak levels were reached at 12 DPI. After the peak levels were reached, they progressively declined and fell to baseline levels (22 DPI). Increased expression of Th2 cytokines (IL-4 and IL-10) first appeared at 14 DPI, peaked at 20 DPI and Th2 cytokine levels were elevated till the end of the study (28 DPI). Levels of serum IFN-gamma detected by a sandwich ELISA correlated well with IFN-gamma gene expression and were detectable at 8-18 DPI. IgM against B. microti was first detected in serum by ELISA at 4 DPI, and peaked at 10 DPI. The levels of IgM subsequently declined but remained positive at low titre till the end of study. IgG against B. microti was first detected at 8 DPI and peak levels were reached at 24 DPI and remained at that level until the end of study. The results of the present study show that Th1 cytokines predominated in the early inflammatory response and might be involved in control of levels of acute parasitaemia whereas the Th2-associated responses, including expression of IL-4 and IL-10 and the production of parasite-specific IgG, might be the functional means for the reduction and clearance of the parasite from the body. It was concluded that an effective vaccine against Babesia spp. should be designed to induce Th1 responses to maintain the parasitaemia at unfulminating levels and also maintain Th2 responses to clear the parasite from the body.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10652120     DOI: 10.1046/j.1365-3024.2000.00279.x

Source DB:  PubMed          Journal:  Parasite Immunol        ISSN: 0141-9838            Impact factor:   2.280


  18 in total

1.  Macrophages are critical for cross-protective immunity conferred by Babesia microti against Babesia rodhaini infection in mice.

Authors:  Yan Li; Mohamad Alaa Terkawi; Yoshifumi Nishikawa; Gabriel Oluga Aboge; Yuzi Luo; Hideo Ooka; Youn-Kyoung Goo; Longzheng Yu; Shinuo Cao; Yongfeng Sun; Junya Yamagishi; Tatsunori Masatani; Naoaki Yokoyama; Ikuo Igarashi; Xuenan Xuan
Journal:  Infect Immun       Date:  2011-11-07       Impact factor: 3.441

Review 2.  Receptor crosstalk: reprogramming B cell receptor signalling to an alternate pathway results in expression and secretion of the autoimmunity-associated cytokine, osteopontin.

Authors:  T L Rothstein; B Guo
Journal:  J Intern Med       Date:  2009-06       Impact factor: 8.989

3.  Macrophages are the determinant of resistance to and outcome of nonlethal Babesia microti infection in mice.

Authors:  Mohamad Alaa Terkawi; Shinuo Cao; Maria S Herbas; Maki Nishimura; Yan Li; Paul Franck Adjou Moumouni; Asadullah Hamid Pyarokhil; Daisuke Kondoh; Nobuo Kitamura; Yoshifumi Nishikawa; Kentaro Kato; Naoaki Yokoyama; Jinlin Zhou; Hiroshi Suzuki; Ikuo Igarashi; Xuenan Xuan
Journal:  Infect Immun       Date:  2014-10-13       Impact factor: 3.441

4.  Recombinant outer membrane protein C of Aeromonas hydrophila elicits mixed immune response and generates agglutinating antibodies.

Authors:  Sunita Kumari Yadav; Jitendra Kumar Meena; Mahima Sharma; Aparna Dixit
Journal:  Immunol Res       Date:  2016-08       Impact factor: 2.829

5.  Development of specific immunoglobulin Ga (IgGa) and IgGb antibodies correlates with control of parasitemia in Babesia equi Infection.

Authors:  Cristina W Cunha; Travis C McGuire; Lowell S Kappmeyer; Stephen A Hines; A Marianela Lopez; Odir A Dellagostin; Donald P Knowles
Journal:  Clin Vaccine Immunol       Date:  2006-02

6.  Suppression of Plasmodium cynomolgi in rhesus macaques by coinfection with Babesia microti.

Authors:  Leonie M van Duivenvoorde; Annemarie Voorberg-van der Wel; Nicole M van der Werff; Gerco Braskamp; Edmond J Remarque; Ivanela Kondova; Clemens H M Kocken; Alan W Thomas
Journal:  Infect Immun       Date:  2010-01-04       Impact factor: 3.441

7.  Cellular immunity, but not gamma interferon, is essential for resolution of Babesia microti infection in BALB/c mice.

Authors:  Michael L Clawson; Natalia Paciorkowski; T V Rajan; Carson La Vake; Conny Pope; Morgan La Vake; Stephen K Wikel; Peter J Krause; Justin D Radolf
Journal:  Infect Immun       Date:  2002-09       Impact factor: 3.441

Review 8.  Human babesiosis.

Authors:  Edouard Vannier; Benjamin E Gewurz; Peter J Krause
Journal:  Infect Dis Clin North Am       Date:  2008-09       Impact factor: 5.982

Review 9.  Investigating disease severity in an animal model of concurrent babesiosis and Lyme disease.

Authors:  Purnima Bhanot; Nikhat Parveen
Journal:  Int J Parasitol       Date:  2018-10-24       Impact factor: 3.981

10.  Robust adaptive immune response against Babesia microti infection marked by low parasitemia in a murine model of sickle cell disease.

Authors:  Woelsung Yi; Weili Bao; Marilis Rodriguez; Yunfeng Liu; Manpreet Singh; Vijendra Ramlall; Jeny R Cursino-Santos; Hui Zhong; Catherine M Elton; Gavin J Wright; Avital Mendelson; Xiuli An; Cheryl A Lobo; Karina Yazdanbakhsh
Journal:  Blood Adv       Date:  2018-12-11
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.