scholarly journals ESAT-6/CFP-10 Fusion Protein and Peptides for Optimal Diagnosis of Mycobacterium tuberculosis Infection by Ex Vivo Enzyme-Linked Immunospot Assay in The Gambia

2005 ◽  
Vol 43 (5) ◽  
pp. 2070-2074 ◽  
Author(s):  
P. C. Hill ◽  
D. Jackson-Sillah ◽  
A. Fox ◽  
K. L. M. C. Franken ◽  
M. D. Lugos ◽  
...  
Vaccine ◽  
2005 ◽  
Vol 23 (21) ◽  
pp. 2740-2750 ◽  
Author(s):  
Jan A.M. Langermans ◽  
T. Mark Doherty ◽  
Richard A.W. Vervenne ◽  
Tridia van der Laan ◽  
Konstantin Lyashchenko ◽  
...  

2014 ◽  
Vol 21 (11) ◽  
pp. 1600-1600
Author(s):  
Leonardo Silva de Araujo ◽  
Fernanda Carvalho de Queiroz Mello ◽  
Nidai de Bárbara Moreira da Silva ◽  
Janaina Aparecida Medeiros Leung ◽  
Silvia Maria Almeida Machado ◽  
...  

2018 ◽  
Vol 26 (3) ◽  
pp. 822-833 ◽  
Author(s):  
Peter Hart ◽  
Alastair Copland ◽  
Gil Reynolds Diogo ◽  
Shane Harris ◽  
Ralf Spallek ◽  
...  

2012 ◽  
Vol 45 (1) ◽  
pp. 134-137 ◽  
Author(s):  
Paulo Antas ◽  
Steven Holland ◽  
Timothy Sterling

Interleukin 8 (CXCL8) is an autocrine chemokine specific for the chemoattraction and activation of granulocytes, NKT cells and T lymphocytes. Patients with tuberculosis and latent Mycobacterium tuberculosis infection were assessed for the spontaneous expression of CXCR1 (CD128) and CXCR2 on lymphocytes and monocytes. Compared with ex vivo profiles, increased spontaneous CXCR2 expression and normal CXCR1 expression were found on lymphocytes in two out of 59 individuals. Monocytes showed normal ex vivo profiles for both receptors. After stimulation with purified protein derivative, the in vitro levels of CXCL8 were below the median levels of all patients with prior tuberculosis. Spontaneous CXCR2 modulation did not cause notable variation in the in vitro levels of CXCL8.


Sign in / Sign up

Export Citation Format

Share Document