{"id":3009,"date":"2026-11-10T11:48:35","date_gmt":"2026-11-10T11:48:35","guid":{"rendered":"https:\/\/innotub.eu\/?p=3009"},"modified":"2026-11-10T11:48:36","modified_gmt":"2026-11-10T11:48:36","slug":"three-tuberculosis-vaccine-candidates-reduce-lesions-and-bacterial-load-in-goats","status":"publish","type":"post","link":"https:\/\/innotub.eu\/en\/three-tuberculosis-vaccine-candidates-reduce-lesions-and-bacterial-load-in-goats\/","title":{"rendered":"Three tuberculosis vaccine candidates reduce lesions and bacterial load in goats"},"content":{"rendered":"\n<p>Vaccination represents a promising tool to complement programmes for the control and eradication of animal tuberculosis, particularly in regions where strategies based on the diagnosis and culling of infected animals have failed to eliminate the disease or are not feasible. However, for their use to be feasible, vaccines must not only be effective but also compatible with diagnostic techniques.<\/p>\n\n<p>In a previous study carried out by members of the INNOTUB II network, a preliminary assessment of the efficacy and diagnostic interference of different prototypes was conducted in a mouse model. The research included a live vaccine, vaccines based on heat-inactivated mycobacteria and others inactivated by bacteriophages; the latter were designed to maintain an antigenic profile more similar to that of live bacteria than that obtained through heat treatment, which results in uncontrolled denaturation of these antigens. Based on the results, some of the most promising candidates were selected for further characterisation of their performance against tuberculosis in infected goats.<\/p>\n\n<p>In <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/42800088\/\">this study, recently published in the journal <em>Vaccine<\/em><\/a>, researchers from NEIKER and IRTA-CReSA have investigated the effects of three vaccine candidates on disease progression, bacterial load and the immune response in goats infected with <em>Mycobacterium caprae<\/em>, focusing on their protective efficacy and diagnostic interference. The vaccines evaluated were one based on heat-inactivated <em>Mycobacterium bovis<\/em> (HIMB), another based on phage-inactivated <em>M. caprae<\/em> (PIMC) and a live vaccine derived from <em>Mycobacterium microti<\/em> (LMM).<\/p>\n\n<p>The severity of total lesions was significantly reduced in vaccinated animals compared with infected animals that were not immunised. Furthermore, some of the vaccines induced beneficial effects on other parameters associated with disease progression, such as a reduction in bacterial load, the volume of lesions in affected lymph nodes, lung tissue mineralisation, or the spread of infection beyond the site of bacterial entry.<\/p>\n\n<p>The other key aspect in enabling the use of vaccines in animals undergoing diagnostic tests for animal tuberculosis is to prevent them from causing interference, that is, cross-reactions that lead to false positives. All three candidate vaccines showed slight interference when the official test, known as the interferon-gamma release assay, was carried out using conventional tuberculins. However, vaccination with any of them was compatible with this same technique when defined antigens designed to differentiate vaccinated animals from those that were genuinely infected were used; this is known as the DIVA (Differentiating Infected from Vaccinated Animals) strategy.<\/p>\n\n<p>The results indicate that vaccination with any of the three prototypes evaluated helps to improve the response to M. caprae infection, although the effects were more pronounced with the HIMB and LMM vaccines. The HIMB prototype stood out for its ability to reduce the bacterial load and enhance the innate immune response, whilst also causing minimal interference in diagnostic tests, particularly when DIVA reagents were used. For its part, LMM demonstrated excellent compatibility with DIVA diagnostic strategies and a marked reduction in lesions and bacterial presence, positioning it as a promising alternative, despite its potential biosafety concerns as it is not an inactivated vaccine. The PIMC prototype also produced positive effects on several of the parameters analysed, albeit to a somewhat lesser extent. However, this first version still has technical limitations related to the loss of antigenic material during the phage inactivation process, an aspect that is currently being optimised.<\/p>\n\n<p>Overall, the results obtained with these vaccines justify further studies to explore and consolidate their usefulness as complementary tools in the control of animal tuberculosis.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Vaccination represents a promising tool to complement programmes for the control and...<\/p>\n","protected":false},"author":4,"featured_media":3016,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[44,17],"tags":[],"class_list":["post-3009","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-actuality","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Three tuberculosis vaccine candidates reduce lesions and bacterial load in goats &#187; 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