Lower female survival from an opportunistic infection reveals progesterone-driven sex bias in trained immunity.

Immune responses differ between females and males, although such sex-based variance is incompletely understood. Observing that bacteremia of the opportunistic pathogen Burkholderia gladioli caused many more deaths of female than male mice bearing genetic deficiencies in adaptive immunity, we determined that this was associated with sex bias in the innate immune memory response called trained immunity. Female attenuation of trained immunity varies with estrous cycle stage and correlates with serum progesterone, a hormone that decreases glycolytic capacity and recall cytokine secretion induced by antigen non-specific stimuli. Progesterone receptor antagonism rescues female trained immune responses and survival from controlled B. gladioli infection to magnitudes similar to those of males. These data demonstrate progesterone-dependent sex bias in trained immunity where attenuation of female responses is associated with survival outcomes from opportunistic infection.

STING controls T cell memory fitness during infection through T cell-intrinsic and IDO-dependent mechanisms.

Stimulator of interferon genes (STING) signaling has been extensively studied in inflammatory diseases and cancer, while its role in T cell responses to infection is unclear. Using Listeria monocytogenes strains engineered to induce different levels of c-di-AMP, we found that high STING signals impaired T cell memory upon infection via increased Bim levels and apoptosis. Unexpectedly, reduction of TCR signal strength or T cell-STING expression decreased Bim expression, T cell apoptosis, and recovered T cell memory. We found that TCR signal intensity coupled STING signal strength to the unfolded protein response (UPR) and T cell survival. Under strong STING signaling, Indoleamine-pyrrole 2,3-dioxygenase (IDO) inhibition also reduced apoptosis and led to a recovery of T cell memory in STING sufficient CD8 T cells. Thus, STING signaling regulates CD8 T cell memory fitness through both cell-intrinsic and extrinsic mechanisms. These studies provide insight into how IDO and STING therapies could improve long-term T cell protective immunity.

Early expression of mature αß TCR in CD4-CD8- T cell progenitors enables MHC to drive development of T-ALL bearing NOTCH mutations.

During normal T cell development in mouse and human, a low-frequency population of immature CD4-CD8- double-negative (DN) thymocytes expresses early, mature αß T cell antigen receptor (TCR). We report that these early αß TCR+ DN (EADN) cells are DN3b-DN4 stage and require CD3δ but not major histocompatibility complex (MHC) for their generation/detection. When MHC - is present, however, EADN cells can respond to it, displaying a degree of coreceptor-independent MHC reactivity not typical of mature, conventional αß T cells. We found these data to be connected with observations that EADN cells were susceptible to T cell acute lymphoblastic leukemia (T-ALL) transformation in both humans and mice. Using the OT-1 TCR transgenic system to model EADN-stage αß TCR expression, we found that EADN leukemogenesis required MHC to induce development of T-ALL bearing NOTCH1 mutations. This leukemia-driving MHC requirement could be lost, however, upon passaging the tumors in vivo, even when matching MHC was continuously present in recipient animals and on the tumor cells themselves. These data demonstrate that MHC:TCR signaling can be required to initiate a cancer phenotype from an understudied developmental state that appears to be represented in the mouse and human disease spectrum.

Physician-patient alignment in satisfaction with psoriatic arthritis treatment in Latin America.

INTRODUCTION: Physician-patient misalignment may exist in real-life clinical practice. We aimed to assess physician and patient treatment satisfaction levels and associated degree of misalignment in psoriatic arthritis (PsA). METHOD: Data from a cross-sectional survey of patients and their physicians conducted in Latin America were analyzed. Physician-reported and patient-reported satisfaction levels with current PsA treatment, alignment in satisfaction levels, and factors associated with satisfaction misalignment were assessed through bivariable and multivariable regression analyses. RESULTS: A total of 179 physician-patient pairs were analyzed. Physicians reported satisfaction with current disease control in 87.7% (n = 157) of cases; patients reported satisfaction in 91.1% (n = 163 of cases). A total of 82.1% of physician-patient pairs were aligned. Compared with aligned patients, misaligned patients were older and more likely to have moderate or severe disease, deteriorating or unstable disease, a past hospital procedure, current or past psoriasis symptoms, greater current pain, a current acute episode, poorer health and quality of life, greater impairment, poorer medication compliance, to consider PsA a major daily burden, and to believe that PsA treatments were ineffective. Misaligned patients were less likely to be in remission. Logistic regression analysis revealed that misaligned patients were older, and more likely to consider PsA a major daily burden and PsA treatments as ineffective. CONCLUSIONS: High levels of treatment satisfaction and alignment were observed among PsA patients and their physicians in Latin America. Patients in this study nevertheless experienced a considerable clinical and quality-of-life burden, especially the misaligned patients. Addressing misalignment may lead to improved PsA disease control.Key points• High treatment satisfaction was observed among PsA patients and their treating physicians in Latin America.• Patients experienced a considerable clinical and quality-of-life burden, especially the misaligned patients.• One-fifth of physician-patient pairs were misaligned regarding satisfaction.• Understanding and addressing misalignment may improve outcomes in this patient population.

Breaking tolerance with engineered class I antigen-presenting molecules.

Successful efforts to activate T cells capable of recognizing weak cancer-associated self-antigens have employed altered peptide antigens to activate T cell responses capable of cross-reacting on native tumor-associated self. A limitation of this approach is the requirement for detailed knowledge about the altered self-peptide ligands used in these vaccines. In the current study we considered allorecognition as an approach for activating CTL capable of recognizing weak or self-antigens in the context of self-MHC. Nonself antigen-presenting molecules typically contain polymorphisms that influence interactions with the bound peptide and TCR interface. Recognition of these nonself structures results in peptide-dependent alloimmunity. Alloreactive T cells target their inducing alloantigens as well as third-party alloantigens but generally fail to target self-antigens. Certain residues located on the alpha-1/2 domains of class I antigen-presenting molecules primarily interface with TCR. These residues are more conserved within and across species than are residues that determine peptide antigen binding properties. Class I variants designed with amino acid substitutions at key positions within the conserved helical structures are shown to provide strong activating signals to alloreactive CD8 T cells while avoiding changes in naturally bound peptide ligands. Importantly, CTL activated in this manner can break self-tolerance by reacting to self-peptides presented by native MHC. The ability to activate self-tolerant T cells capable of cross-reacting on self-peptide-MHC in vivo represents an approach for inducing autoimmunity, with possible application in cancer vaccines.

Differences in the replicative capacities of clinical isolates of dengue virus in C6/36 cells and in urban populations of Aedes aegypti from Colombia, South America

ABSTRACT Dengue, the most prevalent arboviral disease worldwide, is caused by any of the four dengue virus (DENV) serotypes that co-circulate constantly in hyperendemic areas such as Medellin (Colombia), and these serotypes are transmitted by mosquitoes of the genus Aedes. In this study, we evaluated the replicative capacity of strains isolated in Medellin between 2003 and 2007 in C6/36 cells and in colonies of Aedes aegypti collected during 2010-2011 from high or low-incidence areas within the same city. The phylogenetic analysis grouped isolates according to the predominant genotypes found in the Americas, and the in vitro characterization showed differences in the morphological changes induced by the isolates of each of the isolated serotypes compared to the reference serotypes. In vitro replicative capacity studies demonstrated that genomic copy number increased at four days post-infection and that cell viability decreased significantly compared to the control for all serotypes. The largest number of genomic copies in C6/36 was produced by DENV-2, followed by DENV-1 and DENV-4; DENV-3 produced the smallest number of genomic copies and had the smallest negative effect on cell viability. Finally, differences in the in vivo replication of intercolonial serotypes between the Rockefeller colony and the field colonies and among the intracolonial serotypes were found. The replication of DENV-2 at 7 and 14 days in both high- and low-incidence colonies was higher than that of the other serotypes, and replication of DENV-3 in the mosquito colonies was the most stable on the days evaluated. Our results support the notion that replication and, possibly, DENV transmission and severity depend on many factors, including serotype and vector characteristics.

IL-12 Signals through the TCR To Support CD8 Innate Immune Responses.

CD8 T cells must integrate antigenic and inflammatory signals to differentiate into efficient effector and memory T cells able to protect us from infections. The mechanisms by which TCR signaling and proinflammatory cytokine receptor signaling cooperate in these processes are poorly defined. In this study, we show that IL-12 and other proinflammatory cytokines transduce signals through the TCR signalosome in a manner that requires Fyn activity and self-peptide-MHC (self-pMHC) interactions. This mechanism is crucial for CD8 innate T cell functions. Loss of Fyn activity or blockade of self-pMHC interactions severely impaired CD8 T cell IFN-γ and NKG2D expression, proliferation, and cytotoxicity upon cytokine-mediated bystander activation. Most importantly, in the absence of self-pMHC interactions, CD8 memory T cells fail to undergo bystander activation upon an unrelated infection. Thus, CD8 T cell bystander activation, although independent of cognate Ag, still requires self-pMHC and TCR signaling.

Purification of Messenger Ribonucleoprotein Particles via a Tagged Nascent Polypeptide.

The cytoplasmic fates of mRNAs are influenced by interactions between RNA-binding proteins and cis regulatory motifs. In the cytoplasm, mRNAs are present as messenger ribonucleoprotein particles, which include not only proteins that bind directly to the mRNA, but also additional proteins that are recruited via protein-protein interactions. Many labs have sought to purify such particles from cells, with limited success. We here describe a simple two-step procedure to purify actively translated mRNAs, with their associated proteins, from polysomes. We use a reporter mRNA that encodes a protein with three streptavidin binding peptides at the N-terminus. The polysomal reporter mRNA, with associated proteins, is purified via binding to a streptavidin matrix. The method takes four days, and can be applied in any cell that can be genetically manipulated. Using Trypanosoma brucei as a model system, we routinely purified 8% of the input reporter mRNA, with roughly 22-fold enrichment relative to un-tagged mRNAs, a final reporter-mRNA:total-mRNA ratio of about 1:10, and a protein purification factor of slightly over 1000-fold. Although the overall reporter mRNP composition is masked by the presence of proteins that are associated with many polysomal mRNAs, our method can be used to detect association of an RNA-binding protein that binds to specifically to a reporter mRNA.

Maternal IL-6 can cause T-cell-mediated juvenile alopecia by non-scarring follicular dystrophy in mice.

Aiming to decipher immunological mechanisms of the autoimmune disorder alopecia areata (AA), we hypothesized that interleukin-6 (IL-6) might be associated with juvenile-onset AA, for which there is currently no experimental model. Upon intramuscular transgenesis to overexpress IL-6 in pregnant female C57BL/6 (B6) mice, we found that the offspring displayed an initial normal and complete juvenile hair growth cycle, but developed alopecia around postnatal day 18. This alopecia was patchy and reversible (non-scarring) and was associated with upregulation of Ulbp1 expression, the only mouse homolog of the human AA-associated ULBP3 gene. Alopecia was also associated with inflammatory infiltration of hair follicles by lymphocytes, including alpha-beta T cells, which contributed to surface hair loss. Despite these apparently shared traits with AA, lesions were dominated by follicular dystrophy that was atypical of human AA disease, sharing some traits consistent with B6 alopecia and dermatitis. Additionally, juvenile-onset alopecia was followed by complete, spontaneous recovery of surface hair, without recurrence of hair loss. Prolonging exposure to IL-6 prolonged the time to recovery, but once recovered, repeating high-dose IL-6 exposure de novo did not re-induce alopecia. These data suggest that although substantial molecular and cellular pathways may be shared, functionally similar alopecia disorders can occur via distinct pathological mechanisms.

Co-potentiation of antigen recognition: A mechanism to boost weak T cell responses and provide immunotherapy in vivo.

Adaptive immunity is mediated by antigen receptors that can induce weak or strong immune responses depending on the nature of the antigen that is bound. In T lymphocytes, antigen recognition triggers signal transduction by clustering T cell receptor (TCR)/CD3 multiprotein complexes. In addition, it hypothesized that biophysical changes induced in TCR/CD3 that accompany receptor engagement may contribute to signal intensity. Nonclustering monovalent TCR/CD3 engagement is functionally inert despite the fact that it may induce changes in conformational arrangement or in the flexibility of receptor subunits. We report that the intrinsically inert monovalent engagement of TCR/CD3 can specifically enhance physiologic T cell responses to weak antigens in vitro and in vivo without stimulating antigen-unengaged T cells and without interrupting T cell responses to strong antigens, an effect that we term as "co-potentiation." We identified Mono-7D6-Fab, which biophysically altered TCR/CD3 when bound and functionally enhanced immune reactivity to several weak antigens in vitro, including a gp100-derived peptide associated with melanoma. In vivo, Mono-7D6-Fab induced T cell antigen-dependent therapeutic responses against melanoma lung metastases, an effect that synergized with other anti-melanoma immunotherapies to significantly improve outcome and survival. We conclude that Mono-7D6-Fab directly co-potentiated TCR/CD3 engagement by weak antigens and that such concept can be translated into an immunotherapeutic design. The co-potentiation principle may be applicable to other receptors that could be regulated by otherwise inert compounds whose latent potency is only invoked in concert with specific physiologic ligands.

Detection of constant domain of human T cell antigen receptor alpha-chain via novel monoclonal antibody 7F18.

The αß T cell antigen receptor (TCR) endows T lymphocytes with immune specificity and controls their effector functions. Each person possesses a vast repertoire of TCRs that is generated by the well-studied processes of somatic recombination and thymic selection. While many antibodies specific for TCRß variable domains are available, antibodies specific for human TCRα are rare. We now report a novel monoclonal antibody, 7F18, which binds to human TCRα constant region, with specificity for a denatured epitope that can be visualized by SDS-PAGE followed by Western blot. Both immature and mature TCR α-chain products can be visualized, making 7F18 potentially applicable to various biochemical assays of multiprotein complex assembly and maturation. This new monoclonal antibody provides a tool that can potentially facilitate the biochemical analysis of comprehensive populations of human αß TCR complexes that need not be limited to small subsets of the repertoire.

Situación de salud bucal y estado protésico del paciente edentado bimaxilar que acude a la Facultad de Odontología de la Universidad de Antioquia: un estudio piloto / Oral health profile and denture status of bimaxillary edentulous patients treated at universidad de antioquia’s school of dentistry: a pilot study

Introducción: este estudio tuvo como objetivo general analizar la situación de salud bucal y el estado protésico en unamuestra de pacientes edentados bimaxilares atendidos en la clínica del adulto de la Facultad de Odontología de la Universidad de Antioquia. Métodos: estudio descriptivo en 54 pacientes que consultaron a la institución en el periodo 2008-2010. Se consideraron lassiguientes variables: edad, sexo, estrato socioeconómico, nivel educativo, frecuencia de cepillado, utilización de enjuagues, limpieza de la mucosa, remoción nocturna de la prótesis, presencia de estomatitis, úlceras, aumento fibroso, porosidades, pigmentaciones, cálculos, fracturas, dientes caídos, desgaste dentario y grado de satisfacción con el aparato protésico. Se describieron las variables mencionadas por sexo y pruebas Chi cuadrado para observar significancias estadísticas. Resultados: la mayoría de la población estudiada se ubicó en estratos socioeconómicos y niveles educativos bajos. El 48% presentó algún tipo de estomatitis en el arco superior. El 46% se retiran ambas prótesis en la noche, con mayor proporción en las mujeres (58%). Los cálculos fueron el hallazgo más importante en cuanto al estado protésico, presentándose en el 79% en la prótesis inferior. Casi el 80% de la población examinada estaba satisfecha con la prótesis total superior y el 44% con la inferior. Conclusión: los resultados encontrados reflejaron la falta de mantenimiento y controlde la situación de estos pacientes, así como deficiencias en los hábitos de higiene bucal y de las prótesis, situación que no concuerda con la alta satisfacción encontrada.

Introduction: the main objective of this study was to analyze oral health conditions and denture status of a sample of bimaxillary edentulous patients treated at the adult clinic of Universidad de Antioquia’s School of Dentistry. Methods: this was adescriptive study on 54 patients seeking consultation between 2008 and 2010. The following variables were considered: age, gender, socioeconomic level, education level, frequency of brushing, mouthwash use, mucosa cleansing, nightly removal of prosthesis, presence of stomatitis, ulcers, fibrous increase, porosities, pigmentations, calculi, fractures, lost teeth, dental wear, and level of satisfaction withthe prosthetics apparatus. These variables were described by gender and Chi Square tests in order to observe statistical significances. Results: most of the studied population come from lower socioeconomic groups and have low education levels. 48% of this populationpresented some kind of upper arch stomatitis. 46% of them remove both prostheses at night, with a greater proportion among women (58%). Calculi were the most important finding in terms of denture status, as it occurred in 79% of lower prostheses. Almost 80% of the assessed population was satisfied with the upper denture, while 44% were satisfied with the lower one. Conclusions: the findings suggest lack of care and control of these patients’ situation, as well as deficiencies in terms of hygiene habits on both the mouth and the prosthesis —a situation that does not match the high levels of satisfaction found.

Multiplex IP-FCM (immunoprecipitation-flow cytometry): Principles and guidelines for assessing physiologic protein-protein interactions in multiprotein complexes.

There is significant interest in the development of methods with the potential to increase access to 'the interactome' for both experimental and clinical applications. Immunoprecipitation detected by flow cytometry (IP-FCM) is a robust, biochemical method that can be used for measuring physiologic protein-protein interactions (PPI) in multiprotein complexes (MPC) with high sensitivity. Because it is based on antibody-mediated capture of protein complexes onto microspheres, IP-FCM is potentially compatible with a multiplex platform that could allow simultaneous assessment of many physiologic PPI. Here, we consider the principles of ambient analyte conditions (AAC) and inter-bead independence, and provide a template set of experiments showing how to convert singleplex IP-FCM to multiplex IP-FCM, including assays to confirm the validity of the experimental conditions for data acquisition. We conclude that singleplex IP-FCM can be successfully upgraded to multiplex format, and propose that the unique strengths of multiplex IP-FCM make it a method that is likely to facilitate the acquisition of new PPI data from primary cell sources.

Actualización en diagnóstico del dengue: evolución de las técnicas y su aplicación real en la clínica / Update on dengue diagnosis: techniques evolution and their clinical application

Resumen: El dengue es la enfermedad viral transmitida por vectores de mayor importancia en el mundo. Debido a que hasta el momento no existe una vacuna licenciada para la prevención de la infección ni una terapia específica para controlar la enfermedad, el diagnóstico temprano y específico resulta ser una herramienta de vital importancia para brindar un tratamiento rápido y oportuno al paciente. Aunque hace más de seis décadas se dispone de una variedad de técnicas de laboratorio para el diagnóstico de esta enfermedad, es frecuente encontrar que noexista un consenso en el personal o en las entidades colombianas encargadas del diagnóstico de laboratorio sobre las ventajas y las limitaciones de estas técnicas, lo que dificulta dichodiagnóstico. Adicionalmente, debido a que la mayoría de técnicas que se usan se basan en la respuesta inmune frente al virus, y se pueden presentar reacciones cruzadas con otros virusgenéticamente relacionados, la posibilidad de falsos positivos es alta. Principalmente, por estarazón, en los últimos años ha aumentado el desarrollo y la validación de técnicas moleculares,ya que son más sensibles, específicas y rápidas que las técnicas celulares e inmunológicas.Teniendo en cuenta estos antecedentes, se hace necesario comparar a la luz de la literatura disponible la utilidad real de las técnicas de laboratorio existentes, clasificándolas en celulares,inmunológicas y moleculares.

Abstract: Dengue is the vector-borne viral disease of major importance in the world. Because so far there is no licensed vaccine that can be used to prevent the infection and there is no specific antiviral treatment, the early and specific diagnosis is a powerful tool to provide prompt and timely management of the patient. Despite during more than six decades there has been available a wide variety of laboratory techniques that can be used for the diagnosis of dengue, there is often lack of a consensus among the people or entities responsible of the diagnosis about the advantages and disadvantages of these techniques; for this reason, the diagnosis of dengue is more difficult. Moreover, taking into account that most of the techniques used are based on the immune response against dengue virus, and a cross reactivity with other viruses genetically related could be possible; the possibility of false positives is high. Accordingly, in recent years the development and validation of molecular techniques has increased, as they are more sensitive, specific and rapid than the cellular and immunological techniques. Therefore, it is necessary to compare the usefulness of laboratory techniques to dengue diagnosis, such as cellular, immunological and molecular tests.

Historia de la enfermedad de Devic / History of Devic's disease

En este escrito hacemos una completa revisión de la enfermedad de Devic, desde sus primeras descripciones por Eugene Devic, hasta el concepto actual, donde es considerada una neuromielitis óptica. Exponemos las diferentes formas de presentación de la neuromielitis óptica así como los hallazgos clínicos y de laboratorio que permiten diferenciar esta entidad de la esclerosis múltiple, tarea que muchas veces no es fácil de realizar por la semejanza en la presentación clínica. Sin embargo es importante su diferenciación porque el tratamiento y el pronóstico difieren entre estas dos enfermedades. No obstante, el descubrimiento de los anticuerpos IgG anti NMO, dirigidos contra los canales de agua de acuaporina 4 fueron fundamentales en tal diferenciación. Realizamos una mención especial sobre la enfermedad de Devic y el lupus y finalmente hacemos unas notas sobre el tratamiento disponible para esta patología.

In this paper we do a complete review of Devic's disease, from its first descriptions by Eugene Devic, to the current concept, which is considered a neuromyelitis optica (NMO). We present the different forms of presentation of NMO as well as clinical and laboratory findings that distinguish this entity from multiple sclerosis, a task that frequently is not easy to perform because of the similarity in clinical presentation. Its differentiation is important because the treatment and prognosis differ between these two diseases. However the discovery of NMO IgG antibodies directed against aquaporin-4 water channels was a critical step in such differentiation. We made special mention of Devic's disease and lupus, and finally make some notes on the available treatment for this pathology.

Basal and antigen-induced exposure of the proline-rich sequence in CD3ε.

The CD3ε cytoplasmic tail contains a conserved proline-rich sequence (PRS) that influences TCR-CD3 expression and signaling. Although the PRS can bind the SH3.1 domain of the cytosolic adapter Nck, whether the PRS is constitutively available for Nck binding or instead represents a cryptic motif that is exposed via conformational change upon TCR-CD3 engagement (CD3Δc) is currently unresolved. Furthermore, the extent to which a cis-acting CD3ε basic amino acid-rich stretch (BRS), with its unique phosphoinositide-binding capability, might impact PRS accessibility is not clear. In this study, we found that freshly harvested primary thymocytes expressed low to moderate basal levels of Nck-accessible PRS ("open-CD3"), although most TCR-CD3 complexes were inaccessible to Nck ("closed-CD3"). Ag presentation in vivo induced open-CD3, accounting for half of the basal level found in thymocytes from MHC(+) mice. Additional stimulation with either anti-CD3 Abs or peptide-MHC ligands further elevated open-CD3 above basal levels, consistent with a model wherein antigenic engagement induces maximum PRS exposure. We also found that the open-CD3 conformation induced by APCs outlasted the time of ligand occupancy, marking receptors that had been engaged. Finally, CD3ε BRS-phosphoinositide interactions played no role in either adoption of the initial closed-CD3 conformation or induction of open-CD3 by Ab stimulation. Thus, a basal level of open-CD3 is succeeded by a higher, induced level upon TCR-CD3 engagement, involving CD3Δc and prolonged accessibility of the CD3ε PRS to Nck.

El lado oscuro de la sinusitis Presentación de un caso con complicación cerebral / The dark side of sinusitis Report of a case with cerebral complication

La celulitis orbitaria es una infrecuente y potencialmente fatal condición, asociada a trauma ocular o infecciones del tracto respiratorio superior, especialmente sinusitis. Dentro de las complicaciones asociadas se describe el compromiso de sistema nervioso central incluyendo meningitis, trombosis del seno cavernoso y formación de absceso, los cuales se dan con mayor frecuencia en niños y adolescentes. Presentamos el caso de un joven de 20 años quien presentó como complicación un empiema cerebral, denotando la importancia de la tomografía computarizada y el valor del manejo antibiótico y quirúrgico precoz, ya que los resultados fueron satisfactorios ante la ausencia de secuelas (Acta Med Colomb 2010; 35:135-138).

Orbital cellulitis is a rare and potentially fatal condition associated with ocular trauma or upper respiratory tract infections, especially sinusitis. Associated complications include central nervous system involvement including meningitis, cavernous sinus thrombosis and abscess formation which occurs most frequently in children and adolescents. We report the case of a 20 year old man with cerebral empyema as a complication, denoting the importance of computed tomography and the value of appropriate antibiotic therapy and early surgical management, since the results were satisfactory due to the absence of sequelae (Acta Med Colomb 2010; 35:135-138).

Competencia vectorial: consideraciones entomológicas y suinfluencia sobre la epidemiología del dengue / Vector competence: entomological considerations and its implications on the epidemiology of dengue

Las enfermedades transmitidas por vectores constituyen un complejo problema de salud en el ámbito mundial, especialmente en áreas tropicales y subtropicales, que por sus condiciones ambientales favorecen la supervivencia del vector. El dengue es la principal enfermedad transmitida por vectores en el mundo, cuyo agente etiológico es el Virus Dengue, el cual es transmitido por la picadura de mosquitos hematófagos de la especie Aedes aegypti. La interacción virus-vector es esencial para una transmisión efectiva y depende de factores tanto virales como vectoriales. Entre los factores relacionados con el vector, la competencia vectorial es considerada de gran importancia, pues se refiere a la capacidad intrínseca del vector para infectarse con el virus, permitir su replicación y posteriormente su transmisión a un huésped susceptible. A su vez, la habilidad para ser un buen vector depende principalmente de barreras naturales a la infección, barreras inmunológicas y presencia de receptores específicos para el virus. Todas estas características, sumadas a las características propias del virus, favorecerán o no la transmisión del mismo. Un estudio integral dela relación virus-vector permitirá comprender sus implicaciones en la epidemiología de la enfermedad. Estos temas han sido revisados en el presente documento, discutiendo su importancia dentro del contexto entomológico y epidemiológico.

Vector-borne diseases are a serious problem in public health, especially in tropical and subtropical areas where environmental conditions favor the survival and expansion of vectors into new habitats. Dengue fever is one of the most important vector-borne diseases transmitted by arthropods (arbovirosis) worldwide. The etiologic agent of the disease is the dengue virus, which is transmitted by the bite of bloodsucking Aedes aegypti mosquitoes. The virus-vector interaction is essential for the efficient transmission of the disease, and depends on both, viral factors and vector competence or intrinsic vector capacity to be infected with the virus. Vector competence allows virus replication and subsequent transmission to susceptible hosts. Factors that influence vector capacity include: natural barriers to infection, immunological defenses as well as the presence of receptors for the virus. All these factors inaddition to the viral characteristics will determine the degree of transmission. There is a need for a better understanding of the virus-vector relationship and its epidemiological implications. These issues are addressed in this article.

Analysis of the CD33-related siglec family reveals that Siglec-9 is an endocytic receptor expressed on subsets of acute myeloid leukemia cells and absent from normal hematopoietic progenitors.

CD33 (Siglec-3) is expressed on most acute myeloid leukemia (AML) cells and is currently being exploited as a therapeutic target. The purpose of this study was to investigate the expression pattern and potential utility of the seven recently described CD33-related siglecs as markers in AML. Besides CD33, Siglec-9 was the most highly expressed, particularly on AML cells with features of monocytic differentiation that also expressed Siglecs-5 and -7. Siglec-9 was absent from normal bone marrow myeloid progenitors but present on monocytic precursors. Using primary AML cells or transfected rat basophilic leukemia cells, Siglec-9 mediated rapid endocytosis of anti-Siglec-9 mAb. In contrast to CD33 and Siglec-5, levels of soluble Siglec-9 were low or undetectable in bone marrow plasma from AML patients and serum from normal donors. These features suggest that Siglec-9 provides not only a useful marker for certain subsets of AML, but also a potential therapeutic target.

The CD3epsilon proline-rich sequence, and its interaction with Nck, is not required for T cell development and function.

The CD3epsilon proline-rich sequence (PRS) binds to the cytosolic adaptor molecule Nck after TCR ligation. It has been proposed that this interaction is essential for immunological synapse formation and T cell activation. To assess the physiological importance of the CD3epsilon PRS, we have generated mice that lack this motif (CD3epsilon.PRS(M)). Pull-down experiments demonstrated the inability of Nck to bind to the CD3epsilon PRS in thymocytes from mutant mice after TCR ligation. Surprisingly, no differences were observed in the number and percentage of T cell subsets in the thymus and spleen, and there was no apparent defect in positive or negative selection. Furthermore, the proliferative response of CD3epsilon.PRS(M) T cells to staphylococcal enterotoxin B and anti-CD3 Ab was normal. TCR surface expression, constitutive internalization, and Ag-induced down-modulation were also normal. These data suggest that the interaction between the CD3epsilon PRS and Nck, or any other Src homology 3 domain-containing molecule, is not essential for T cell development and function.