Vaccination against helminth parasites - the ultimate challenge for vaccinologists?

被引:65
作者
Maizels, RM
Holland, MJ
Falcone, FH
Zang, XX
Yazdanbakhsh, M
机构
[1] Univ Edinburgh, Inst Cell Anim & Populat Biol, Edinburgh EH9 3JT, Midlothian, Scotland
[2] Leiden Univ, Med Ctr, Dept Parasitol, Leiden, Netherlands
基金
英国惠康基金;
关键词
D O I
10.1111/j.1600-065X.1999.tb01345.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Helminths are multicellular pathogens which infect vast numbers of human and animal hosts, causing widspread chronic disease and morbidity. Vaccination against these parasites requires more than identification of effective target antigens, because without understanding the immunology of the host-parasite relationship, ineffective immune mechanisms may be invoked, and there is a danger of amplifying immunopathogenic responses. The fundamental features of the immune response to helminths are therefore summarised in the context of vaccines to helminth parasites. The contention between type-1 and type-2 responses is a central issue in helminth infections, which bias the immune system strongly to the type-2 pathway. Evidence from both human and experimental animal infections indicates that both lineages contribute to immunity in differing circumstances, and that a balanced response leads to the most favourable outcome. A diversity of immune mechanisms can be brought to bear on various helminth species, ranging from antibody-independent macrophages, antibody-dependent granulocyte killing, and non-lymphoid actions, particularly in the gut. This diversity is highlighted by analysis of rodent infections, particularly in comparisons of cytokine-depleted and gene-targeted animals. This knowledge of protective mechanisms needs to be combined with a careful choice of parasite antigens for vaccines. Many existing candidates have been selected with host antibodies, rather than T-cell responses, and include a preponderance of highly conserved proteins with similarities to mammalian or invertebrate antigens. Advantage has yet to be taken of parasite genome projects, or of directed searches for novel, parasite-specific antigens and targets expressed only by infective stages and not mature forms which may generate immunopathology. With advances under way in parasite genomics and new vaccine delivery systems offering more rapid assessment and development, there are now excellent opportunities for new antihelminth vaccines.
引用
收藏
页码:125 / 147
页数:23
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共 241 条
[21]  
Bancroft AJ, 1998, J IMMUNOL, V160, P3453
[22]   Phylogeny of Wolbachia in filarial nematodes [J].
Bandi, C ;
Anderson, TJC ;
Genchi, C ;
Blaxter, ML .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1998, 265 (1413) :2407-2413
[23]   Differences between IL-4Rα-deficient and IL-4-deficient mice reveal a role for IL-13 in the regulation of Th2 responses [J].
Barner, M ;
Mohrs, M ;
Brombacher, F ;
Kopf, M .
CURRENT BIOLOGY, 1998, 8 (11) :669-672
[24]   PROTECTION AGAINST MYCOPLASMA-INFECTION USING EXPRESSION-LIBRARY IMMUNIZATION [J].
BARRY, MA ;
LAI, WC ;
JOHNSTON, SA .
NATURE, 1995, 377 (6550) :632-635
[25]   UNDERSTANDING CHRONIC NEMATODE INFECTIONS - EVOLUTIONARY CONSIDERATIONS, CURRENT HYPOTHESES AND THE WAY FORWARD [J].
BEHNKE, JM ;
BARNARD, CJ ;
WAKELIN, D .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1992, 22 (07) :861-907
[26]   Schistosomiasis vaccines: Research to development [J].
Bergquist, NR ;
Colley, DG .
PARASITOLOGY TODAY, 1998, 14 (03) :99-104
[27]   Enhanced response to a DNA vaccine encoding a fusion antigen that is directed to sites of immune induction [J].
Boyle, JS ;
Brady, JL ;
Lew, AM .
NATURE, 1998, 392 (6674) :408-411
[28]  
Brown T R, 1898, J Exp Med, V3, P315, DOI 10.1084/jem.3.3.315
[29]  
Brunet LR, 1997, J IMMUNOL, V159, P777
[30]   Cytokine interaction and immune responses during Schistosoma mansoni infection [J].
Brunet, LR ;
Dunne, DW ;
Pearce, EJ .
PARASITOLOGY TODAY, 1998, 14 (10) :422-427