Immune responses of cattle vaccinated by various routes with Mycobacterium bovis Bacillus Calmette-Guérin (BCG)

被引:0
作者
Palmer, Mitchell V. [1 ]
Hwang, Soyoun [2 ]
Kanipe, Carly [1 ,3 ]
Putz, Ellie J. [1 ]
Fernandes, Luis Guilherme Virgilio [4 ]
Didkowska, Anna [5 ]
Boggiatto, Paola M. [1 ]
机构
[1] Natl Anim Dis Ctr, Agr Res Serv, Bacterial Dis Livestock Res Unit, 1920 Dayton Ave, Ames, IA 50010 USA
[2] USDA, Ctr Vet Biol Anim & Plant Hlth Inspection Serv, 1920 Dayton Ave, Ames, IA 50010 USA
[3] Iowa State Univ, Coll Vet Med, Immunobiol Grad Program, 1800 Christensen Dr, Ames, IA 50010 USA
[4] Oak Ridge Inst Sci & Educ, 1299 Bethel Valley Rd, Oak Ridge, TN 37830 USA
[5] Warsaw Univ Life Sci SGGW, Inst Vet Med, Dept Food Hyg & Publ Hlth Protect, Nowoursynowska 159, PL-02776 Warsaw, Poland
关键词
BCG; Bovine; Lyophilization; Mycobacteria; Oral; Tuberculosis; Vaccination; CALMETTE-GUERIN VACCINATION; FORMULATION INDUCES RESISTANCE; T-CELL RESPONSES; ORAL VACCINATION; PULMONARY TUBERCULOSIS; PROTECTION; RABIES; ELIMINATION; COMBINATION; EFFICACY;
D O I
10.1186/s12917-024-04452-7
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundMycobacterium bovis BCG is the human tuberculosis vaccine and is the oldest vaccine still in use today with over 4 billion people vaccinated since 1921. The BCG vaccine has also been investigated experimentally in cattle and wildlife by various routes including oral and parenteral. Thus far, oral vaccination studies of cattle have involved liquid BCG or liquid BCG incorporated into a lipid matrix. Lyophilization is an established technique used for stabilizing bioproducts such as vaccines.MethodsIn the current study, cattle were vaccinated in two phases. In each phase, cattle were divided into three groups. Group 1 received BCG injected SQ, Group 2 received liquid BCG delivered to the posterior oral cavity, Group 3 orally consumed lyophilized BCG contained within a gelatin capsule placed within a small amount of a commercial alfalfa product.ResultsNo vaccinated cattle were positive by an interferon gamma release assay. All but 4 animals were negative by tuberculin skin testing prior to vaccination: the 4 non-negative animals being categorized as suspects. Sixteen weeks post-vaccination all but 1 animal was negative, it being categorized as a suspect. An in vitro antigen stimulation assay and flow cytometry were used to detect antigen-specific CD4, CD8 and gamma delta T cell responses following vaccination. Oral vaccination of animals with lyophilized BCG did not result in any increases in the frequency of CD4, CD8 or gamma delta T cell proliferative or IFN-gamma responses at any of the time points analyzed in either phase 1 or 2. In contrast, vaccination with BCG SQ and liquid BCG delivered to the posterior pharynx, resulted in an increase in the frequency of proliferating and IFN-gamma-producing CD4 T cells with peak responses at 9-12 weeks post-vaccination. Similar to oral lyophilized BCG vaccinated animals, we did not observe any significant increases in the frequency of CD8 and gamma delta T cell proliferative and IFN-gamma responses following SQ or oral liquid vaccinated animals.ConclusionsThese data would suggest that vaccination with oral lyophilized BCG does not induce a measurable, antigen-specific cell mediated responses in the periphery, when compared to BCG administered SQ or liquid BCG administered via the oral route. However, vaccination with either SQ or liquid BCG delivered to the posterior pharynx does induce measurable CD4 T cell responses in the periphery.
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