Pulmonary tuberculosis (TB) remains one of the most infectious causes of death worldwide. Mycobacterium tuberculosis (M.tb), the causative agent of TB is transmitted via infectious aerosols, and in the majority of cases the bacteria is effectively controlled, by the host, resulting in a chronic latent infection. Currently, the only available vaccine is the Bacillus Calmette-Guérin (BCG), which despite being successful in preventing childhood disseminated forms of TB, has failed to control the adult pulmonary TB epidemic. One of the major contributing factors in the failure of the BCG is that although antigen-specific T cells are present at the time of M.tb infection, the recruitment of such T cells into the site of infection is significantly delayed. This delay, while reduced compared to non-vaccinated hosts, allows the bacteria to replicate unchecked within the lung and establish a “foothold” prior to the arrival of protective T cells and subsequent immune control. Thus, novel initiatives seek to close this “immunological gap” through increasing the level of protective T cell responses within the airway mucosa immediately following M.tb infection. We therefore investigated the impact of deliberate modulation of T cell geography following BCG vaccination on the outcome of pulmonary M.tb infection. In addition, a number of environmental factors are also thought to affect the site of M.tb infection: the respiratory mucosa. However, little is currently known about the effects of environmental exposure to allergens and other substances such as cigarette smoke on the outcome of pulmonary TB. Throughout this thesis we have investigated the mechanisms of immune protection and failure of protection against pulmonary M.tb infection within the respiratory mucosa. / Thesis / Doctor of Philosophy (Medical Science)

No description available.

Asthma is defined as reversible airflow obstruction and an estimated 1-in-3 Canadians will be diagnosed over their lifetime. Many clinical phenotypes of asthma exist, but allergic asthma is the most common presentation. Despite effective therapies, approximately 65% of Canadian asthmatics have poorly controlled disease. Thus, there remains pressing need to develop disease modifying therapies. Allergen-specific immunotherapy (SIT) is a disease-modifying therapy for allergic disease that consists of repeatedly administering doses of allergen, to an allergic individual; over 100 years of clinical use, SIT has been demonstrated to reduce symptoms of disease both during and after cessation of therapy. Widespread clinical uptake of SIT has been limited by the risk of developing anaphylaxis as a response to therapy. Peptide immunotherapy is a derivation of SIT, that attempts to retain the disease-modifying benefits, while lessening the risk of anaphylaxis, by treating subjects with allergen-derived T-cell peptide epitopes. Peptide immunotherapy has been demonstrated to reduce symptoms of allergic disease in treated subjects; however, it remains unknown how administration of a single (or several) T-cell epitopes can modulate immune responses to entire complex allergens. Additionally, how genetic diversity in peptide epitope presentation effects the development of immune tolerance is unknown. In this thesis, we sought to characterize these mechanisms of peptide immunotherapy; the hypothesis was, “The induction of immunosuppression by peptide immunotherapy involves the infectious spread of tolerance beyond the treatment epitope, and is dependent upon treatment peptide dose and affinity to MHC”. Through the definition of these mechanistic traits we hoped to expedite and inform the design of future peptide based therapeutics. The studies presented within this thesis examine the topic of immune modulation of allergic disease in mouse models, and have focused upon broadly pertinent characteristics of immune modulation, such as the number, dose and affinity of immunomodulatory epitopes. / Thesis / Doctor of Philosophy (PhD) / Asthma is a disease of the airways that can cause difficulties in breathing. In some people, asthma develops because their immune system reacts in an uncontrolled manner to common environmental proteins, called allergens. Whole allergen immunotherapy is a treatment for asthma, where asthmatic people are injected with doses of allergen until their immune system no longer responds to (or ‘tolerates’) the allergen. In some people, injection of allergen can lead to a life-threatening immune response known as ‘anaphylaxis’. Peptide-immunotherapy is a form of whole allergen immunotherapy where people are given small fragments of the allergen (a ‘peptide’) rather than the whole allergen. The benefit of peptide immunotherapy is that the treatment peptides are too small to cause anaphylaxis, but remain large enough to teach the immune system. In this thesis, we examined how treatment with small peptides teaches the immune system to tolerate the larger and more complex whole allergen.

O ozônio, forma triatômica do oxigênio, tem sido amplamente estudado ao longo dos anos. Sua aplicação destaca-se devido ao seu alto poder oxidativo na ação contra bactérias, fungos, protozoários e vírus. A alta instabilidade faz com que o gás transforme-se em oxigênio após determinado tempo, não liberando resíduos no ambiente. Também tem sua aplicação estudada de forma a aprimorar o sistema circulatório, produzindo aumento na oxigenação tecidual, estimulando a produção de antioxidantes endógenos e causando efeito imunomodulador (com a estimulação da liberação de citocinas). Foi o objetivo deste trabalho a organização das informações sobre o ozônio empregado na Medicina Veterinária e Odontologia Humana, principalmente suas aplicações como antimicrobiano, para esclarecer a importância de suas utilizações e fornecer subsídios para que a ozonioterapia possa ser utilizada na Odontologia Veterinária. Assim, com base na literatura, foi possível concluir que a ozonioterapia constitui proposta coadjuvante promissora diante da necessidade do controle da infecção, além da ação imunomoduladora que pode ser empregada nas mais variadas situações da prática clínica. / Ozone, the triatomic form of oxygen, has been widely studied over the years. With a very oxidative potential, acts against bacteria, fungi, protozoa and viruses. The high instability, after a few minutes makes it return to the oxygen form. This is important because of the non residual effect on the environment. The ozone has also an immune modulating effect, stimulating the release of endogenous anti-oxidants and acts in the circulation system inducing to an increase on oxygen tissue levels. This research aimed to gather information about ozone, particularly the antimicrobial effect, raising the importance of the applications, aiming a possible use of the ozone in Veterinary Dentistry. Therefore, it is possible to conclude that the ozone therapy can be an important adjuvant to infectious diseases control, and can be used in different types of clinical applications.

O ozônio, forma triatômica do oxigênio, tem sido amplamente estudado ao longo dos anos. Sua aplicação destaca-se devido ao seu alto poder oxidativo na ação contra bactérias, fungos, protozoários e vírus. A alta instabilidade faz com que o gás transforme-se em oxigênio após determinado tempo, não liberando resíduos no ambiente. Também tem sua aplicação estudada de forma a aprimorar o sistema circulatório, produzindo aumento na oxigenação tecidual, estimulando a produção de antioxidantes endógenos e causando efeito imunomodulador (com a estimulação da liberação de citocinas). Foi o objetivo deste trabalho a organização das informações sobre o ozônio empregado na Medicina Veterinária e Odontologia Humana, principalmente suas aplicações como antimicrobiano, para esclarecer a importância de suas utilizações e fornecer subsídios para que a ozonioterapia possa ser utilizada na Odontologia Veterinária. Assim, com base na literatura, foi possível concluir que a ozonioterapia constitui proposta coadjuvante promissora diante da necessidade do controle da infecção, além da ação imunomoduladora que pode ser empregada nas mais variadas situações da prática clínica. / Ozone, the triatomic form of oxygen, has been widely studied over the years. With a very oxidative potential, acts against bacteria, fungi, protozoa and viruses. The high instability, after a few minutes makes it return to the oxygen form. This is important because of the non residual effect on the environment. The ozone has also an immune modulating effect, stimulating the release of endogenous anti-oxidants and acts in the circulation system inducing to an increase on oxygen tissue levels. This research aimed to gather information about ozone, particularly the antimicrobial effect, raising the importance of the applications, aiming a possible use of the ozone in Veterinary Dentistry. Therefore, it is possible to conclude that the ozone therapy can be an important adjuvant to infectious diseases control, and can be used in different types of clinical applications.

Type 1 diabetes (T1D) results from the destruction of pancreatic β-cells caused by an altered immune balance in the pancreatic microenvironment. In humans as well as in mouse models, T cells are well recognized as key orchestrators of T1D, which is characterized by T helper (Th) 1 and Th17 cell bias and/or low/defective T-regulatory cells (Treg), and culminates in cytotoxic T-cell (CTL)-mediated destruction of β-cells. Refitting of immune cells toward the non-inflammatory phenotype in the pancreas may represent a way to prevent/treat T1D. Recently we developed a unique spontaneous humanized mouse model of type 1 diabetes, wherein mouse MHC-II molecules were replaced by human DQ8, and β-cells were made to express human glutamic acid decarboxylase (GAD) 65 auto-antigen. The mice spontaneously developed T1D resembling the human disease. Humanized T1D mice showed hyperglycemic (250-300 mg/dl) symptoms by the 4th week of life. The diabetogenic T cells (CD4, CD8) present in our model are GAD65 antigen-specific in nature. Intermolecular antigen spreading recorded during 3rd-6th week of age is like that observed in the human preclinical period of T1D. In this paper, we tested our hypothesis in our spontaneous humanized T1D mouse model. We targeted two cell-signaling pathways and their inhibitions: eIF5A pathway inhibition influences T helper cell dynamics toward the non-inflammatory phenotype and Notch signaling inhibition enrich Tregs and targets auto-reactive CTLs, rescues the pancreatic islet structure, and increases the functionality of β-cells in terms of insulin production. We report that inhibition of (eIF5A + Notch) signaling mediates suppression of diabetogenic T cells by inducing plasticity in CD4 + T cells co-expressing IL-17 and IFNγ (IL-17 + IFNγ +) toward the Treg cells phenotype.

Introduction: The incidence of food allergy has increased substantially in developed countries, with limited treatment and/or prevention options. Milk oligosaccharides have shown to modulate immune responses by serving as prebiotic substrates for the intestinal microbiota. However, some studies suggest that oligosaccharides may exert direct immunomodulatory effects, suggesting their therapeutic potential in preventing allergic diseases. We hypothesized that specific milk oligosaccharides including 6’sialyllactose, 2’fucosylactose, 3’sialyllactose and lacto-N-neotetraose may directly exert immunomodulatory effects on dendritic cells (DCs) and epithelial cells (ECs) by altering their phenotype and/or function in vitro. Methods: The effects of milk oligosaccharides (MOs) on bone-marrow derived DCs and the T84 and MODE-K epithelial cell lines were studied via direct treatment, in vitro. The expression of immunomodulatory cytokines and maturation markers were assessed to measure the effect of MOs on DC phenotype. Pro- and anti-inflammatory cytokines as well as NFκB p65 activity were measured to assess the effect of MOs on DC and EC function. In addition, in vitro stimulation of CD23 with IgE-Antigen complexes were used to study the effects of MOs on ECs in relation to allergy. Lastly, inhibitory antibodies for Siglec-F and PPARγ were used to elucidate the mechanism used by specific MOs to exert their effects. Results: Of the oligosaccharides studied, 6’siallylactose has direct immunomodulatory effects on DC phenotype and on DC and EC function at high concentrations. 6’sialyllactose increased DC expression of IL-10 and HO-1; it also increased CpG- and LPS- induced IL-10 release and decreased IL-12p70 release. Blocking the PPARγ receptor with GW9662 resulted in attenuation of this latter effect on IL-12p70 release. 6’sialyllactose reduced TNF-α induced IL-8 to a small but statistically significant extent and mKC to a great extent in T84 and MODE-K cells, respectively. In addition, 6’sialyllactose reduced IgE-Antigen stimulated release of IL-8 and CCL20, as well as NFκB p65 activity. Pre-treatment of cells with GW9662 resulted in attenuation of the effect of 6’SL on IL-8 release and p65 activation. In addition, 2’fucosylactose reduced CCL20 release and NFκB activity substantially, but these effects were not exerted via PPARγ. Conclusion: Some oligosaccharides are able to directly modulate the inflammatory response in DCs and ECs, via pathways involving PPARγ activation and/or NFκB inhibition. / Thesis / Master of Science (MSc)

Il est maintenant bien établi que le microbiote du tractus digestif humain joue un rôle important dans la santé humaine. Pourtant, nous commençons à peine à comprendre les mécanismes moléculaires par lesquels les bactéries agissent sur les cellules hôtes, des connaissances qui pourraient fournir des nouvelles orientations dans le traitement et la prévention de maladies. Cette dernière décennie a vu un développement rapide des études du microbiote intestinal, et à présent des quantités importantes de données métagénomiques ainsi que des centaines de séquences génomiques de bactéries commensales sont disponibles. Ensemble, ces données fournissent une plateforme pour des approches in silico pour l'identification de molécules bactériennes impliquées dans la communication moléculaire avec l'hôte. Le défi consiste à développer des stratégies efficaces d'exploration de données et de validation, permettant de passer de corrélations et prédictions à des interactions bactérie - hôte fonctionnelles, validées expérimentalement. Le travail présenté dans cette thèse vise à démontrer l'importance d'analyses in silico afin d'élargir nos connaissances sur les interactions bactéries - hôtes. Il montre également comment cette information peut être appliquée dans des études fonctionnelles visant à identifier des molécules effectrices bactériennes fonctionnelles. Les principaux résultats peuvent être divisés en trois parties. La première partie traite de l'élaboration et de la validation d'un système hôte - vecteur pour des études de (méta)génomique fonctionnelle. La deuxième partie décrit une étude fonctionnelle où un certain nombre d'effecteurs candidats ont été identifiés parmi les protéines sécrétées et de surface de bactéries à Gram positif par une approche d'exploration in silico. Il décrit également l'application du nouveau système hôte - vecteur pour l'évaluation du rôle de ces candidats dans l'immuno-modulation. Enfin, dans la troisième partie, nous présentons une étude in silico qui a permis l'identification de fonctions bactériennes sur- ou sous-représentées dans une sélection de bactéries à Gram positif du tractus digestif humain. / It is now well established that the human gastrointestinal tract microbiota plays an intricate role in human health. However, we are only beginning to understand the molecular mechanisms by which bacteria act on the host cells, knowledge that could provide new directions in treating and preventing disease. The last decade has seen a rapid development of the gut microbiota field, and presently abundant metagenome data and hundreds of genome sequences of individual commensal bacteria are available. Together, these data provide a platform for in silico mining approaches to identify bacterial molecules involved in communication with the host. The challenge is to develop efficient mining and validation strategies, in order to move from correlations and predictions to experimentally validated functional bacteria – host relationships. The work presented in this thesis aims to demonstrate the importance of in silico analyses to broaden our knowledge on bacteria - host interactions. It also shows how this information can be applied in functional studies aiming to identify functional bacterial effector molecules. The main results can be divided in three parts. The first part deals with the development and validation of a host - vector system for functional (meta)genomics studies. The second part describes a functional study where a number of candidate effectors were identified among secreted and surface-exposed proteins from Gram-positive bacteria using an in silico mining approach. It also describes the application of the newly developed host - vector system to evaluate the role of these candidates in immune modulation. Finally, in the third part we present an in silico study that identified new bacterial functions over- or under-represented in a selection of Gram-positive human gut bacteria.

Submitted by Renata Lopes (renatasil82@gmail.com) on 2016-09-14T12:27:00Z No. of bitstreams: 1 patriciapaivacorsetti.pdf: 2969873 bytes, checksum: f90d3d721f56a1166b3f3bbc78e327a9 (MD5) / Approved for entry into archive by Diamantino Mayra (mayra.diamantino@ufjf.edu.br) on 2016-09-26T20:17:54Z (GMT) No. of bitstreams: 1 patriciapaivacorsetti.pdf: 2969873 bytes, checksum: f90d3d721f56a1166b3f3bbc78e327a9 (MD5) / Made available in DSpace on 2016-09-26T20:17:54Z (GMT). No. of bitstreams: 1 patriciapaivacorsetti.pdf: 2969873 bytes, checksum: f90d3d721f56a1166b3f3bbc78e327a9 (MD5) Previous issue date: 2011-10-07 / Brucella abortus é uma bactéria patogênica Gram-negativa, que causa uma doença crônica em bovinos, humanos e outras espécies denominada brucelose. A habilidade do hospedeiro em montar uma resposta tipo Th1/pró-inflamatória contra a bactéria é crucial para o controle e resolução da infecção. Evidências sugerem que a citocina IFN-γ produzida pelo perfil Th1 é crucial para o controle da infecção em camundongos. A interleucina-10 (IL-10) é conhecida por diminuir a produção de IFNγ in vitro interferindo diretamente no processo da eliminação do patógeno. Durante a infecção pela B. abortus, a IL-10 pode atuar limitando a resposta inflamatória e favorecendo o estabelecimento da infecção persistente em camundongos. O objetivo deste estudo foi avaliar o papel da IL-10 endógena na infecção pela B. abortus. Para acessar o papel da IL-10, camundongos deficientes para IL-10 (IL-10 KO) ou 129 Sv/Ev foram infectados com a cepa S2308 de B. abortus e foram avaliados os númerso de bactérias viáveis recuperadas no baço desses animais. Uma, 2, 3, 6 e 14 semanas após infecção, camundongos IL-10 KO apresentaram menor número de bactérias recuperadas quando comparadas com o grupo controle em todos os tempos de infecção, principalmente em 14 semanas. Adicionalmente, constatou-se por análise de curva de sobrevivência em um período de 14 semanas após infecção que aproximadamente 35% dos camundongos IL-10 KO morrem somente na 2ª ou 3ª semana. Ademais, a produção de IFN-γ, IL-10, IL-17 e TNF-α foi avaliada em esplenócitos dos camundongos infectados quando estimulados in vitro com a B. abortus viva (S2308), morta pelo calor (HKBA), LPS de E. coli ou ConA. Os animais IL-10 KO apresentaram uma maior quantidade de IFN-γ e TNF-α no sobrenadante das células estimuladas com Brucella quando comparada a produção destas citocinas pelas células provenientes dos camundongos 129 Sv/Ev. A citocina IL-17 somente foi produzida pelas células dos animais IL-10 KO em todos os tempos analisados. Adicionalmente, a produção de TNF-α, IL-6, IL-12-p40, NO e IL-10 foram avaliados em macrófagos derivados da medula óssea, dos animais IL-10 KO e 129 Sv/Ev. TNF-α, NO, IL-6 e IL-12 apresentaram aumento nos animais IL-10 KO apenas quando estimulados com HKBA. Entretanto, nos animais 129 Sv/Ev a bactéria viva e morta estimularam a produção de IL-10. Estas mesmas citocinas foram avaliadas em sobrenadante de cultura de células dendríticas derivadas da medula óssea. Níveis mais elevados de TNF-α e IL-12-p40 foram obtidos no sobrenadante de células de animais IL-10 KO quando comparados ao grupo controle, em todos os tempos e estímulos da cinética de infecção. A expressão de TGF-β foi avaliada por PCR em tempo real em células esplênicas nos tempos 0 (não infectado), 1, 2 e 6 semanas de infecção estimulados com a bactéria viva. Na 2ª semana após infecção os animais IL-10 KO expressaram níveis mais elevados de TGF-β em relação ao grupo controle, porém na 6ª semana este perfil é invertido. Adicionalmente, o nível de células CD4+CD25+Foxp3+ (Treg) presente no baço dos animais infectados foi analisado por citometria de fluxo. Esta população encontrouse aumentada nos animais IL-10 KO a partir da 3ª e 6ª semanas após a infecção. Análises histopatológicas descritiva dos fígados destes animais durante toda a cinética de infecção demonstraram a diminuição gradativa dos granulomas nos dois grupos estudados, porém essa redução foi mais eficiente nos camundongos IL-10 KO principalmente na 6ª semana após a infecção considerando-se a área do granuloma, analisada por morfemetria digital, e a recuperação do parênquima hepático. Em conjunto, os dados obtidos neste trabalho suportam que a ausência da produção da IL-10 está associada a uma maior resistência à infecção pela bactéria B. abortus em modelo murino, através do aumento da produção de citocinas próinflamatórias culminando com uma maior eliminação da bactéria e uma resolução mais rápida da patologia tecidual do hospedeiro levando, assim, a um controle efetivo da infecção. / Brucella abortus is a Gram-negative pathogenic bacterium which causes a chronic disease in bovine, humans and others species called brucellosis. The host ability to mount a Th1/pro-inflammatory response against the bacteria is crucial to control and to solve the infection. It is suggested that IFN-γ produced by Th1cells is crucial to control the infection in mice. The interleukin IL-10 is considered to be responsible to decrease the IFN-γ production in vitro interfering directly in the pathogen elimination. During B. abortus infection, IL-10 acts limiting inflammatory response favoring the establishment persistence infection in mice. The goal of this study was evaluated the role of endogenous IL-10 during B. abortus infection. To assess the role of IL-10 in vivo, IL-10 knockout (IL-10 KO) mice or 129 Sv/Ev mice were infected with B. abortus strain S2308 and the number of viable bacteria recovery from the spleen were evaluated. One, 2, 3, 6 and 14 weeks post infection, IL-10 KO mice showed lower number of bacteria in the spleen when compared to wild type mice during all the time points. It was observed the increase of the difference at 14th week post infection. Additionally, it was demonstrated by survival curve in a period of 14 weeks post infection that approximately 35% of IL-10 KO mice died only at 2 or 3 weeks. Furthermore, the IFN-γ, IL-10, IL-17 and TNF-α production were measured in the supernatant from spleen cell culture in vitro when the cells were stimulated with alive B. abortus (S2308), heat killed B. abortus (HKBa), E. coli LPS or ConA. IL-10 KO cells showed greater increase in IFN-γ and TNF-α level in the supernatant from these cells when they were stimulated with Brucella when compared to wild type cells production. IL-17 was only detected in the supernatant from IL-10 KO cells in all time points analyzed. In addition, the TNF-α, IL-6, IL-12-p40, NO and IL-10 levels were evaluated in bone-marrow macrophage derived cell supernatant. TNF-α, NO, IL-6 and IL-12 showed augmented in IL-10 KO cells when stimulated with HKBa. However, only in supernatant from 129 Sv/Ev mice it was observed IL-10 production. In bone-marrow dendritic cell supernatant greater levels of TNF-α and IL-12-p40 were observed in IL-10 KO cells when compared to wild type mice cells during all time points analyzed when the cells were stimulated with all stimulus. The TGF-β expression was evaluated by real time PCR in splenic cells culture at 0 (non-infected cells), 1, 2 and 6 weeks after infection with S2308. At 2 weeks post infection the IL-10 KO cells demonstrated greater increased of TGF-β expression when compared to wild type cells. At 6 weeks post infection the TGF-β expression profile showed inverted. Additionally, the level of CD4+CD25+Foxp3+ (Treg) cells was assessed at spleen of infected mice by flow cytometry during the infection process. This population was increased at 3th and 6th weeks post infection in IL-10 KO mice. Descriptive histopathology analyses were done at liver level demonstrating a gradual diminishment of granuloma in both kinds of analyzed animals. However, the decrease pathology was more effective at IL-10 KO livers considering the granuloma area, measured by digital morphometry, and the hepatic parenchyma recovery. Taken together, the data provided by this work support that the lack of IL-10 is related to higher resistance to B. abortus infection in murine infection throughout the increase production of pro-inflammatory cytokines culminating with better bacteria elimination and a quicker tissue pathological resolution leading to a more effective control of this infection.

O principal crescimento na indústria de alimentos funcionais corresponde ao dos produtos probióticos e prebióticos. A literatura mostra efeitos imunomoduladores de certas cepas probióticas, contudo, os resultados são às vezes controversos e os mecanismos implicados ainda são pouco elucidados. Sabe-se, no entanto que algumas cepas de probióticos aumentam significantemente a liberação de IL-10 e γ-INF modulando a resposta imune, além destas respostas serem de forma mais branda relacionada às bactérias Gram-positivas probióticas do que às Gram-positivas patogênicas. O presente trabalho teve como objetivo geral estudar o efeito do leite probiótico fermentado na resposta imune celular em cólon de camundongos BALB/c. Os objetivos específicos foram: (i) determinar o efeito imunomodulador do leite adicionado de probiótico em camundongos normais, (ii) identificar os tipos celulares implicados na resposta imune específica por citometria de fluxo e, (iii) colocalizá-los nos cortes histológicos. Simultaneamente, a análise e a comparação da resistência do probiótico à digestão gastrintestinal in vitro e a produção de metabólitos bioativos de acordo com os deferentes produtos foi realizada. Foram preparados leites nos quais as variáveis estudadas foram a tecnologia empregada para a produção das formulações (a) leite; (b) água, (c) leite não fermentado; (d) leite fermentado; (e) leite fermentado seguido de pasteurização, usando a mesma concentração da cepa comercial Bifidobacterium animalis subsp. lactis HOWARU HN019. O leite desnatado e a água foram usados como controles. / Functional food industry is in expansion mainly due to probiotic and prebiotic products. Studies have shown some probiotic strains develop immune modulation effect, however, these results are controversial and the mechanisms are not been well understood. Although, some probiotic strains increase IL-10 and γ-INF release modulating immune response, this response is weaker in probiotic strains when compared to pathogenic Gram-positive bacteria. The major aim of the present study was to assess the effect of probiotic fermented milk in cellular immune response of Balb/c mice colon. The specific objectives were: (i) to determine the immunomodulation of the milk added of probiotic in normal mice; (ii) to identify the cellular types implied in immune specific response and, (iii) to colocalize them in histological sections. Besides, the analyze and comparation of the probiotic resistance upon in vitro gastrointestinal and bioactive metabolites release in fermented or unfermented bifido milk using the same matrix, probiotic strain and probiotic dose in CFU. mL-1 were conducted. Dairy products were prepared in which variable form of technological appliance were: (i) milk, (ii) water, (iii) unfermented milk, (iv) fermented milk, and (v) fermented and heat treatment milk, all using Bifidobacterium subsp. lactis HOWARU HN019 strain in the same concentration. The skimmed milk and water were used as controls. The immune effects were evaluated by histological sections and the lymphocytic infiltrated was analyzed by flow citometry and histology.