Immunogenic characterization of a tissue culture-derived vaccine that affords partial protection against avian coccidiosis

被引:12
作者
Brake, DA
Strang, G
Lineberger, JE
Fedor, CH
Clare, R
Banas, TA
Miller, T
机构
[1] Activated Cell Therapy, Mountainview, CA 94043
[2] Merck and Co., West Point, PA 19486
[3] SmithKline Beecham, UW-2110, King of Prussia, PA 19406
[4] SmithKline Beecham, Collegeville, PA 19426-0989
[5] Creative BioMolecules, Hopkintown, MA 01748
[6] Benchmark Biolabs, Box 5423, Lincoln, NE 68505, N 315
[7] Animal Health Biological Discovery, Pfizer Central Research Division, Pfizer Inc., Groton, CT 06340, Eastern Point Road
关键词
coccidiosis; tissue culture; vaccine; immunity; Eimeria;
D O I
10.1093/ps/76.7.974
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The immunogenicity of a tissue culture-derived vaccine generated from an Eimeria tenella-infected cell line in a serologically defined bird line, and the ability to confer protection against homologous challenge in young chicks was examined. The cell Line, SB-CEV-1/F7, was infected with E. tenella sporozoites and the resulting 72-h postinfection cell-free supernatants were adjuvanted and used to immunize Leghorn chicks homozygous for the B-19 haplotype. Peripheral blood and splenic lymphocytes from these immunized birds proliferated in vitro in response to both sporozoite and SB-CEV-1/F7 tissue culture-derived parasite antigens. In addition, splenic immune lymphocytes obtained from birds previously exposed to E. tenella in vivo responded to these tissue culture-derived parasite antigens in vitro. To evaluate the efficacy of the vaccine, (BB19)-B-19 chicks were vaccinated s.c. with adjuvanted 72-h postinfection cell-free supernatants or an ammonium sulfate precipitate derivative thereof, orally boosted, and then subjected to homologous parasite challenge at 10 d of age. The level of protection (body weight gain, cecal lesions) was assessed 6 d after challenge. Performance results from four battery trials demonstrated that vaccinated birds were significantly protected against weight loss compared to unimmunized, challenged controls. In addition, in two of the four trials, vaccinated birds were significantly protected against lesions. These results provide strong evidence that tissue culture-derived parasite antigens obtained from the E. tenella-infected SB-CEV-1/F7 cell line are immunogenic in birds and can provide partial protection against E. tenella clinical coccidiosis.
引用
收藏
页码:974 / 983
页数:10
相关论文
共 31 条
[11]  
Doran D.J., 1982, P229
[12]   THE PURIFICATION OF SPOROCYSTS AND SPOROZOITES FROM EIMERIA-TENELLA OOCYSTS USING PERCOLL DENSITY GRADIENTS [J].
DULSKI, P ;
TURNER, M .
AVIAN DISEASES, 1988, 32 (02) :235-239
[13]  
Fernando M. A., 1990, Coccidiosis of man and domestic animals., P63
[14]   BEHAVIOR OF INVASIVE STAGES OF EIMERIA TENELLA IN IMMUNE FOWL (GALLUS DOMESTICUS) [J].
HORTONSMITH, C ;
LONG, PL ;
PIERCE, AE .
EXPERIMENTAL PARASITOLOGY, 1963, 14 (01) :66-&
[15]   X-IRRADIATION OF EIMERIA-TENELLA OOCYSTS PROVIDES DIRECT EVIDENCE THAT SPOROZOITE INVASION AND EARLY SCHIZONT DEVELOPMENT INDUCE A PROTECTIVE IMMUNE RESPONSE(S) [J].
JENKINS, MC ;
AUGUSTINE, PC ;
DANFORTH, HD ;
BARTA, JR .
INFECTION AND IMMUNITY, 1991, 59 (11) :4042-4048
[16]   DEVELOPMENT OF RESISTANCE TO COCCIDIOSIS IN THE ABSENCE OF MEROGONIC DEVELOPMENT USING X-IRRADIATED EIMERIA-ACERVULINA OOCYSTS [J].
JENKINS, MC ;
AUGUSTINE, PC ;
BARTA, JR ;
CASTLE, MD ;
DANFORTH, HD .
EXPERIMENTAL PARASITOLOGY, 1991, 72 (03) :285-293
[17]   EIMERIA-ACERVULINA - DNA CLONING AND CHARACTERIZATION OF RECOMBINANT SPOROZOITE AND MEROZOITE ANTIGENS [J].
JENKINS, MC ;
LILLEHOJ, HS ;
DAME, JB .
EXPERIMENTAL PARASITOLOGY, 1988, 66 (01) :96-107
[18]   ANTICOCCIDIAL DRUGS - LESION SCORING TECHNIQUES IN BATTERY AND FLOOR-PEN EXPERIMENTS WITH CHICKENS [J].
JOHNSON, J ;
REID, WM .
EXPERIMENTAL PARASITOLOGY, 1970, 28 (01) :30-+
[19]   EFFECTS OF IMMUNE CHICKEN ON ENDOGENOUS STAGES OF EIMERIA TENELLA [J].
LEATHEM, WD ;
BURNS, WC .
JOURNAL OF PARASITOLOGY, 1967, 53 (01) :180-&
[20]  
Lillehoj H. S., 1991, Avian cellular immunology., P155