CHARACTERIZATION OF IMMUNE-RESPONSE TO EIMERIA-TENELLA ANTIGENS IN A NATURAL IMMUNITY MODEL WITH HOSTS WHICH DIFFER SEROLOGICALLY AT THE B-LOCUS OF THE MAJOR HISTOCOMPATIBILITY COMPLEX
Da. Brake et al., CHARACTERIZATION OF IMMUNE-RESPONSE TO EIMERIA-TENELLA ANTIGENS IN A NATURAL IMMUNITY MODEL WITH HOSTS WHICH DIFFER SEROLOGICALLY AT THE B-LOCUS OF THE MAJOR HISTOCOMPATIBILITY COMPLEX, Infection and immunity, 65(4), 1997, pp. 1204-1210
A model to simulate natural immunity to Eimeria tenella was developed
in three chicken lines which differ at the B locus of the major histoc
ompatibility complex, Homozygous, 1-day-old chicks of the (BB19)-B-19,
(BB24)-B-24, or (BB30)-B-30 genotype were trickle immunized by being
orally fed a small infectious dose of E. tenella oocysts for 5 consecu
tive days, These naturally exposed birds were then challenged at diffe
rent times between 5 and 24 days after the final dose, and the level o
f protection was assessed 6 days after challenge, using body weight ga
in and intestinal lesion scores, The duration of immunity in naturally
exposed birds differed among the major histocompatibility complex lin
es, Trickle immunization of the (BB19)-B-19 haplotype afforded the lon
gest and strongest level of protection compared to the other two haplo
types tested, In addition, in vitro splenic and peripheral blood lymph
ocyte proliferative responses in trickle-immunized birds were measured
against sporozoite, merozoite, and tissue culture-derived B. tenella
parasite antigens isolated from the recently described SB-CEV-1/F7 est
ablished cell line, The lymphocytes obtained from (BB19)-B-19 birds tr
ickle immunized responded in vitro to the E. tenella-infected SB-CEV-1
/F7 tissue culture derived parasite antigen, Furthermore, antigen-spec
ific immune responses appeared earlier in immune, challenged (BB19)-B-
19 birds than in their naive, challenged counterparts, The development
of a model simulating natural immunization will serve as a foundation
to further characterize both humoral and cell-mediated responses to E
. tenella tissue culture-derived parasite antigens and to better under
stand host protective immune responses to avian coccidiosis.