Chronic helminth infections may negatively influence immunity against tuberculosis and other diseases of public health importance

被引:70
作者
Elias, Daniel
Britton, Sven
Kassu, Afework
Akuffo, Hannah
机构
[1] ACE Biosci, DK-5220 Odense SOE, Denmark
[2] Ammaeur Hansen Res Inst, Addis Ababa, Ethiopia
[3] Karolinska Inst, Dept Med, Infect Dis Unit, S-10401 Stockholm, Sweden
[4] Karolinska Inst, Dept Microbiol Cell & Tumor Biol, S-10401 Stockholm, Sweden
关键词
helminths; HIV; immune disorder; immunomodulation; tuberculosis;
D O I
10.1586/14787210.5.3.475
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Tuberculosis (TB) has once again become a major public health threat owing to the combined effects of deteriorating socioeconomic situations and the emergence of the HIV/AIDS pandemic. The only vaccine available against TB, although effective in reducing the burden of childhood TB, shows enormous variability in its efficacy against pulmonary TB, which is the most common form of the disease in adults. Most areas of high TB incidence and poor TB vaccine efficacy have a high prevalence of intestinal helminth infections. Such infections have been shown to cause a range of immunomodulation characterized by enhanced T helper 2-type cytokine profile, high immunoglobulin E levels and upregulated regulatory T-cell activity, as well as chronic immune activation. An altered background immune profile could have adverse effects on the outcome of subsequent infections and vaccinations. In support of this hypothesis, studies conducted in animals and humans living in worm-endemic areas have shown that helminths impair resistance against a number of infections of major public health importance, including TB, malaria and HIV/AIDS. Understanding such interactions could assist in the design of vaccines against these diseases.
引用
收藏
页码:475 / 484
页数:10
相关论文
共 99 条
[71]   EFFICACY OF BCG VACCINE AGAINST LEPROSY AND TUBERCULOSIS IN NORTHERN MALAWI [J].
PONNIGHAUS, JM ;
FINE, PEM ;
STERNE, JAC ;
WILSON, RJ ;
MSOSA, E ;
GRUER, PJK ;
JENKINS, PA ;
LUCAS, SB ;
LIOMBA, NG ;
BLISS, L .
LANCET, 1992, 339 (8794) :636-639
[72]  
ROMAGNANI S, 1991, INT J CLIN LAB RES, V21, P152
[73]   Immune responses to tuberculosis in developing countries: implications for new vaccines [J].
Rook, GAW ;
Dheda, K ;
Zumla, A .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (08) :661-667
[74]   Do successful tuberculosis vaccines need to be immunoregulatory rather than merely Th1-boosting? [J].
Rook, GAW ;
Dheda, K ;
Zumla, A .
VACCINE, 2005, 23 (17-18) :2115-2120
[75]   Modulation of human T cell responses and macrophage functions by onchocystatin, a secreted protein of the filarial nematode Onchocerca volvulus [J].
Schönemeyer, A ;
Lucius, R ;
Sonnenburg, B ;
Brattig, N ;
Sabat, R ;
Schilling, K ;
Bradley, J ;
Hartmann, S .
JOURNAL OF IMMUNOLOGY, 2001, 167 (06) :3207-3215
[76]  
Selassie FG, 2000, CLIN EXP ALLERGY, V30, P356, DOI 10.1046/j.1365-2222.2000.00706.x
[77]   CD8+ T cells participate in the memory immune response to Mycobacterium tuberculosis [J].
Serbina, NV ;
Flynn, JL .
INFECTION AND IMMUNITY, 2001, 69 (07) :4320-4328
[78]   Immunomodulation of experimental autoimmune encephalomyelitis by helminth ova immunization [J].
Sewell, D ;
Qing, Z ;
Reinke, E ;
Elliot, D ;
Weinstock, J ;
Sandor, M ;
Fabry, Z .
INTERNATIONAL IMMUNOLOGY, 2003, 15 (01) :59-69
[79]   Immunoregulation of CNS autoimmunity by helminth and mycobacterial infections [J].
Sewell, DL ;
Reinke, EK ;
Hogan, LH ;
Sandor, M ;
Fabry, Z .
IMMUNOLOGY LETTERS, 2002, 82 (1-2) :101-110
[80]   Contribution of CD8+ T cells to gamma interferon production in human tuberculosis [J].
Shams, H ;
Wizel, B ;
Weis, SE ;
Samten, B ;
Barnes, PF .
INFECTION AND IMMUNITY, 2001, 69 (05) :3497-3501