Abstract: Background: Diseases caused by melanized fungi include mycetoma, chromoblastomycosis and phaeohyphomycosis. This broad clinical spectrum depends on the dynamic interactions between etiologic agent and host. The immune status of the host influences on the development of the disease, as, an exemple. phaeohyphomicosis is more frequently observed in immunocompromised patients. Objectives: Examine the histological inflammatory response induced by Fonsecaea pedrosoi in several different strains of mice (BALB/c, C57BL/6, Nude and SCID, and reconstituted Nude). Methods: Fonsecaea pedrosoi was cultivated on agar gel and a fragment of this gel was implanted subcutaneously in the abdominal region of female adult mice. After infection has been obtained, tissue fragment was studied histopathologically. Results: There were significant changes across the strains, with the nodular lesion more persistent in Nude and SCID mice, whereas in immunocompetent mice the lesion progressed to ulceration and healing. The histopathological analysis showed a significant acute inflammatory reaction which consisted mainly of neutrophils in the initial phase that was subsequently followed by a tuberculoid type granuloma in immunocompetent mice. Study limitations: There is no a suitable animal model for chromoblastomycosis. Conclusions: The neutrophilic infiltration had an important role in the containment of infection to prevent fungal spreading, including in immunodeficient mice. The fungal elimination was dependent on T lymphocytes. The re-exposure of C57BL/6 mice to Fonsecaea pedrosoi caused a delay in resolving the infection, and appearance of muriform cells, which may indicate that re-exposure to fungi, might lead to chronicity of infection.

A caracterização da origem, propriedades, funções e destino das células representam objetivo fundamental para a compreensão dos fenômenos fisiológicos e patológicos. Apesar da grande quantidade de conhecimentos relativos às diversas características das células de mamíferos, muitas delas, inclusive células B-1, são pouco entendidas. Depois de mostrar que as células B-1 podem ser cultivadas e amplificadas in vitro, uma série de experimentos visando esclarecer as propriedades dessas células puderam ser feitos em nosso laboratório nos últimos 10 anos. Assim, pudemos demonstrar que células B-1 residem principalmente nas cavidades peritoneal e pleural do camundongo, migram para focos inflamatórios distantes, coalescem para formar células gigantes e participam na formação de granulomas, tanto in vitro como in vivo. São também capazes de apresentar antígenos a células responsivas e são dotadas de propriedades imuno-regulatórias. Mostramos ainda que estas células favorecem diferentes tipos de infecções bem como o crescimento e metastatização tumoral. Esses resultados sugerem que células B-1 devem exercer papel central na imunidade como um todo.

Characterization of the origin, properties, functions and fate of cells is a fundamental task for the understanding of physiological and pathological phenomena. Despite the bulk of knowledge concerning the diverse characteristics of mammalian cells, some of them, such as B-1 cells, are still poorly understood. Here we report the results obtained in our laboratory on these cells in the last 10 years. After showing that B-1 cells could be cultured and amplified in vitro, a series of experiments were performed with these cells. They showed that B1 cells reside mostly in the peritoneal and pleural cavities, migrate to distant inflammatory foci, coalesce to form giant cells and participate in granuloma formation, both in vitro and in vivo. They are also able to present antigens to immunologically responsive cells and are endowed with regulatory properties. Further, we have also shown that these cells facilitate different types of infection as well as tumor growth and spreading. These data are presently reviewed pointing to a pivotal role that these cells may play in innate and acquired immunity.

OBJETIVO: Investigar a integração do transplante heterólogo de quelóide na bolsa jugal do hamster (Mesocricetus auratus). MÉTODOS: A amostragem consiste de 18 hamsters machos, heterogênicos, com 10 a 14 semanas de idade. Fragmentos de quelóide foram obtidos de cicatrizes queloidianas da região mamária de paciente adulta parda. Cada hamster foi enxertado em ambas as bolsas com fragmentos de quelóide, totalizando 36 fragmentos enxertados. Os animais foram distribuídos em 6 grupos para exame dos fragmentos enxertados, com 5, 12, 21, 42, 84 e 168 dias. Uma avaliação macroscópica é realizada comparando a bolsa contendo o fragmento enxertado em cada período com a mesma bolsa no pós-operatório imediato, mediante a comparação de fotografias padronizadas. À microscopia, considera-se a presença de vasos sangüíneos no tecido conjuntivo do fragmento enxertado como critério de integração do mesmo. Outros eventos, como secreção de queratina, presença de infiltrados celulares e aspecto do epitélio e das fibras colágenas do quelóide, também são observados. RESULTADOS: A macroscopia revela intensa vascularização na bolsa até 12 dias de enxertia, e a presença constante de pigmentação castanho-escura nos fragmentos de quelóide enxertados. Na microscopia constata-se a integração dos fragmentos de quelóide pela presença de capilares sangüíneos no tecido conjuntivo. Observa-se, também, a presença de intenso infiltrado celular do tipo inflamatório até 12 dias, a permanência do epitélio do quelóide até 21 dias, e o aparecimento de melanócitos a partir de 42 dias. CONCLUSÃO: A bolsa jugal do hamster representa, a priori, modelo experimental para investigação do quelóide.

PURPOSE: To study the integration of keloid heterograft in hamster (Mesocricetus auratus) cheek pouch. METHODS: The sample is formed by 18 male hamsters, heterogenic ones, aged between 10 and 14 weeks. Keloid fragments were obtained from keloid scars of the breast region of adult female mulatto patient. Each hamster received keloid fragments into both of its pouches, in a total of 36 grafted fragments. Animals were distributed into 6 groups for having their grafts assessed in the days 5, 12, 21, 42, 84, and 168. A macroscopic assessment is performed by comparing the pouch containing the grafted fragment, at each time point, with the same pouch in the immediate post surgical moment through a comparison of standardized photographs. Under microscope, the presence of blood vases is considered within the conjunctive tissue of the grafted fragment, as a criterion of its integration. Other events, as keratin secretion, the presence of cellular infiltrated, epithelium and keloid collagen fibers aspects are also analyzed. RESULTS: Macroscopy reveals intensive vascularization of the pouch up to 12 days from the transplantation and the presence of constant dark brown pigmentation on the grafted keloid fragments. In microscopy, the integration of keloid fragments is considered by the presence of blood capillary vases within conjunctive tissue. The presence of intensive cellular inflammatory type infiltrated up to 12 days is also observed, as well as the remaining of keloid epithelium up to 21 days, and the appearing of melanocytes from the day 42. CONCLUSION: Hamster cheek pouch represents, a priori, an experimental model for the investigation of keloid.

O hamster sírio dourado (Mesocricetus auratus) possui no subepitélio de suas bolsas jugais um "Local de Privilégio Imunológico", permitindo a integração de homo e heteroenxertos. Este artigo descreve as características anatômicas e histológicas desse local, assim como os aspectos relativos as suas propriedades imunológicas. Cita, também, as vantagens desse modelo experimental sobre outros modelos portadores, naturais ou induzidos, de imunodeficiência. Com base nessas vantagens, e também baseado na literatura, tem o intuito de estabelecer esse modelo, mediante a realização de heteroenxertos, como uma outra opção para investigar distúrbios cicatriciais, como o quelóide, e doenças de interesse em Cirurgia Plástica, como lesões cutâneas benignas e neoplasias malignas como carcinomas e melanoma cutâneo. Tece, ainda, considerações sobre perspectivas de aplicações desse modelo, ainda bastante desconhecido entre a classe médica brasileira.

Syrian golden hamster (Mesocricetus auratus) has in its cheek pouches sub-epithelium an "Immunologically Privileged Site" which allows the integration of homo- and heterologous graft. This paper describes some anatomical and histological characteristics of that site, as well as analyzes aspects related with its immune properties. It also focuses the advantages of this experimental model over other models which are natural or induced carriers of immunodeficiency. Based on both these advantages and literature, this study aims to establish this model, through the performance of heterologous graft, as another option for the investigation of scar disturbances, as keloids and other diseases which may interest Plastic Surgery, as benign cutaneous lesions, and malignant neoplasias such as skin carcinomas and melanomas. The work also addresses perspectives for using this model, which still is a source scarcely known by Brazilian medical class.

Descrever a integração dos enxertos de pele total humana e quelóide na bolsa jugal do hamster (Mesocricetus auratus), cujo subepitélio é, naturalmente, um "Local de Privilégio Imunológico". Foram transplantados fragmentos, de pele humana normal e de quelóide, obtidos da região mamária de pacientes pardas, no subepitélio da bolsa jugal in situ. O procedimento operatório, e de preparo das bolsas enxertadas para exame microscópico em vários períodos de transplante, foi padronizado. Verificou-se a integração dos fragmentos enxertados de pele humana e de quelóide em períodos tardios (84 dias), uma vez que a avaliação microscópica revelou a presença de vasos sangüíneos no tecido conjuntivo dos fragmentos enxertados. Foi também possível observar, nos fragmentos enxertados, o epitélio, o aparecimento de infiltrado celular incipiente, secreção epitelial de queratina, presença de melanócitos e alterações tardias no aspecto das fibras colágenas do tecido conjuntivo. Os resultados, em conjunto, permitem estabelecer o subepitélio da bolsa jugal do hamster como modelo experimental para investigação da fisiologia de tranplantes heterólogos de pele total humana e quelóide com epitélio.

To describe the integration process of grafts of total human skin and keloid in hamster (Mesocricetus auratus) cheek pouch, whose sub-epithelium is naturally an "Immunologically Privileged Site". Fragments of human normal skin and keloid from the breast region of mulatto female patients were transplanted into the cheek pouch subepithelium in situ. Surgical procedure and grafted pouches for microscopic exam at several time points of the transplantation were standardized. The integration of grafted fragments of human skin and keloid was seen in late periods (84 days) since the microscopic assessment showed the presence of blood vases within the conjunctive tissue of grafted fragments. It was also possible to see among the grafted fragments the epithelium, the appearing of early cellular infiltrated, epithelial secretion of keratin, the presence of melanocytes, and delayed changes on the aspect of collagen fibers of conjunctive tissue. Pooled results allow to define hamster cheek pouch sub-epithelium as an experimental model to investigating heterologous graft physiology of human total skin and keloid with epithelium.

Diferentes espécies de animais vertebrados e invertebrados têm sido usados em investigação biomédica experimental. Neste trabalho é apresentada uma breve revisão sobre o uso do suíno em pesquisa biomedica e sobre as similaridades da anatomia, fisiologia, bioquímica e imunologia desta espécie com aquelas do homem. É também revisto o desenvolvimento do minipig nos anos 60 e os sucessos obtidos com este modelo animal nas mais diversas áreas da medicina experimental. Finalmente, são descritas as características básicas de uma colônia de minipigs desenvolvida pelo autor (Minipig br1). São descritas as condições de alimentação desses animais, como são mantidos, vacinados e selecionados. Pesam de 10-15 quilos com seis meses de idade e de 30-37 quilos com onze meses. A possível contribuição desse modelo animal para o desenvolvimento da cirurgia experimental e para outras áreas de experimentação animal no país é discutida.

Different species of vertebrate and invertebrate animals have been used in experimental investigation. In this report a brief review on the use of swine in biomedical research and the similarities of the anatomy, physiology, biochemistry and immunology of this specie with those of man is presented. It is also reviewed the development in the 60th of the minipig and the achievements obtained with this animal model in distinct areas of experimental medicine. Finally, the basic characteristics of a colony of minipigs developed by the author are described. The conditions these animals are feed, housed, vaccinated and breed are described. They weight from 10-15 kilos when six months of age and from 30-37 kilos with 11 months of age. The possible contribution of this animal model for the development of experimental surgery and other areas of animal experimentation in this country is discussed.

OBJETIVO: Descrever a integração de enxertos de pele total humana no subepitélio da bolsa jugal do hamster (Mesocricetus auratus). MÉTODOS: A amostragem consistiu de 18 hamsters machos, exogâmicos, com 10 a 14 semanas de idade. Fragmentos de pele humana normal foram obtidos de pele excedente de mastoplastia redutora de paciente parda. Cada hamster foi enxertado em ambas as bolsas com fragmentos de pele, perfazendo um total de 36 fragmentos enxertados. Os animais foram distribuídos, em 6 grupos, para exame dos fragmentos enxertados com 5, 12, 21, 42, 84 e 168 dias. Uma avaliação macroscópica foi realizada comparando a bolsa contendo o fragmento enxertado em cada período com a mesma bolsa no pós-operatório imediato, mediante fotografias padronizadas. Na avaliação microscópica foi adotado como critério de integração a presença de vasos sangüíneos na derme dos enxertos. Observou-se também a presença de queratina, melanócitos, infiltrado celular e aspecto do tecido conjuntivo. RESULTADOS: Na avaliação macroscópica foi observada uma reação vascular em torno dos fragmentos até 12 dias do implante, e a presença de pigmentação castanho-escura a partir de 42 dias. À microscopia, integraram-se 80,64% dos fragmentos enxertados, inclusive no grupo de 168 dias. Observou-se infiltrado celular inflamatório até 12 dias, a presença de melanócitos a partir de 42 dias e uma hialinização do tecido conjuntivo após 84 dias. CONCLUSÕES: Fragmentos de pele humana integram-se no tecido celular subcutâneo da bolsa jugal do hamster, mantêm-se vascularizados por 168 dias, e conservam o epitélio íntegro até 21 dias. O subepitélio da bolsa representa modelo experimental de investigação da fisiologia de pele humana ex vivo.

PURPOSE: To describe the integration of total human skin into hamster (Mesocricetus auratus) cheek pouch. METHODS: The sample was formed by 18 male hamsters, outbred, aging between 10 and 14 weeks. Fragments of normal human skin were obtained from reduction mastoplasty of a mulatto woman patient. Each hamster was grafted into both pouches with skin fragments, in a total of 36 fragments grafted. Animals were distributed into 6 groups for examination of the grafted fragments at the days 5, 12, 21, 42, 84, and 168. One macroscopic assessment was performed by comparing the pouch containing the grafted fragment in each period with the same pouch in the immediate post surgical, following standardized photographs. In the microscopic assessment, as an integration criterion of the grafted skin fragments, the presence of blood vases within the dermis was adopted. The presence of keratin, melanocytes, cellular infiltrated, and the aspect of conjunctive tissue was also observed. RESULTS: In the macroscopic evaluation a vascular reaction in fragments up to 12 days and the presence of dark brown pigmentation up to 42 days were observed. Under microscope 80.64% of grafted fragments were integrated, including in the group of 168 days. An inflammatory cellular infiltrated was observed up to 12 days, the presence of melanocytes from 42 days and a subcutaneous cellular tissue hyalinization after 84 days were seen. CONCLUSIONS: Fragments of human skin integrate into the hamster pouch, they remain vascularized for 168 days and preserve the whole epithelium up to 21 days. The pouch sub-epithelium represents an experimental model to investigating human skin physiology ex vivo.

OBJETIVO: Descrever a integração do transplante heterólogo de quelóide no subepitélio da bolsa jugal do hamster (Mesocricetus auratus). MÉTODOS: A amostragem consiste de 18 hamsters machos, não isogênicos, com 10 a 14 semanas de idade. Fragmentos de quelóide foram obtidos de cicatrizes queloideanas da região mamária de paciente adulta parda. Cada hamster foi enxertado em ambas as bolsas com fragmentos de quelóide, totalizando 36 fragmentos enxertados. Os animais foram distribuídos, em 6 grupos, para exame dos fragmentos enxertados com 5, 12, 21, 42, 84 e 168 dias. Uma avaliação macroscópica é realizada comparando a bolsa contendo o fragmento enxertado em cada período com a mesma bolsa no pós-operatório imediato, mediante a comparação de fotografias padronizadas. À microscopia, considera-se a presença de vasos sangüíneos no tecido conjuntivo do fragmento enxertado como critério de integração do mesmo. Outros eventos, como secreção de queratina, presença de infiltrados celulares e aspecto do epitélio e das fibras colágenas do quelóide, também são observados. RESULTADOS: A macroscopia revela intensa vascularização na bolsa até 12 dias de enxertia, e a presença constante de pigmentação castanho-escura nos fragmentos de quelóide enxertados. Na microscopia constata-se a integração dos fragmentos de quelóide pela presença de capilares sangüíneos no tecido conjuntivo. Observa-se, também, a presença de intenso infiltrado celular do tipo inflamatório até 12 dias, a permanência do epitélio do quelóide até 21 dias, e o aparecimento de melanócitos a partir de 42 dias. CONCLUSÃO: A bolsa jugal do hamster representa, a priori, modelo experimental para investigação do quelóide.

PURPOSE: To describe the integration of keloid heterograft into hamster (Mesocricetus auratus) sub-epithelium. METHODS: The sample is formed by 18 male hamsters, not isogenetic ones, aged between 10 and 14 weeks. Keloid fragments were obtained from keloid scars of the breast region of adult female mulatto patient. Each hamster received keloid fragments into both of its pouches, in a total of 36 grafted fragments. Animals were distributed into 6 groups for having their grafts assessed in the days 5, 12, 21, 42, 84, and 168. A macroscopic assessment is performed by comparing the pouch containing the grafted fragment, at each time point, with the same pouch in the immediate post surgical moment through a comparison of standardized photographs. Under microscope, the presence of blood vases is considered within the conjunctive tissue of the grafted fragment, as a criterion of its integration. Other events, as keratin secretion, the presence of cellular infiltrated, and epithelium and keloid collagen fibers aspects are also analyzed. RESULTS: Macroscopy reveals intensive vascularization of the pouch up to 12 days from the transplant, and the presence of constant dark brown pigmentation on the grafted keloid fragments. In microscopy the integration of keloid fragments is found by the presence of blood capillary vases within conjunctive tissue. The presence of intensive cellular inflammatory type infiltrated up to 12 days is also observed, as well as the remaining of keloid epithelium up to 21 days, and the appearing of melanocytes from the day 42. CONCLUSION: Hamster cheek pouch represents, a priori, an experimental model for the investigation of keloid.

The authors present morphogenetic and biomechanical approaches on the concept of the Schistosoma mansoni granulomas, considering them as organoid structures that depend on cellular adhesion and sorting, forming rearrangement into hierarchical concentric layers, creating tension-dependent structures, aiming to acquire round form, since this is the minimal energy form, in which opposing forces pull in equally from all directions and are in balance. From the morphogenetic point of view, the granulomas function as little organs, presenting maturative and involutional stages in their development with final disappearance (pre-granulomatous stages, subdivided in: weakly and/or initial reactive and exudative; granulomatous stages: exudative-productive, productive and involutional). A model for the development of granulomas was suggested, according to the following stages: encapsulating, focal histolysis, fiber production, orientation and compacting and involution and desintegration. The authors concluded that schistosomal granuloma is not a tangled web of individual cells and fibers, but an organized structure composed by host and parasite components, which is not formed to attack the miracidia, but functions as an hybrid interface between two different phylogenetic beings.

We summarize here the main characteristics of a novel model of pulmonary hypersensitivity. Mice were immunized with a subcutaneous implant of a fragment of heat solidified chicken egg white and 14 days later challenged with ovalbumin given either by aerosol or by intratracheal instillation. This procedure induces a persistent eosinophilic lung inflammation, a marked bone marrow eosinophilia, and Th2-type isotypic profile with histopathological findings that resemble human asthma. Further, this model is simple to perform, reproducible in different strains of mice, does not require adjuvants nor multiple boosters. Based on these characteristics we propose it as a suitable murine model of allergic eosinophilic lung inflammation.