anti-T Antibodies Research Articles

Clinical and laboratory characteristics of Toxocara canis infection among children in Ho Chi Minh City, Vietnam.

This study determines the clinical and paraclinical characteristics of children with Toxocara canis infection and serum eosinophil cut-off values for predicting toxocariasis in the group displaying symptoms of itching, urticaria and erythema. A cross-sectional study was conducted during March and April 2023 with a sample size of 986 children aged 3-15 y. In total, 140 (14.2%) of the 986 participants had anti-T canis antibodies. The most frequently experienced symptoms in this group were itching (10.1%), abdominal pain (8.2%) and urticaria (3.3%). The rate of IgE increased (37%), and the rates of mild and high eosinophilia were 38% and 2.2%, respectively. There were significant differences in IgE concentration and eosinophil count, and for both IgE concentration and eosinophil count between the two groups with and without toxocariasis. The optimal threshold for eosinophil to predict toxocariasis was 0.38 K/µL, with itching, urticaria and erythema resulting in a sensitivity of 61.5%, a specificity of 82.1% and a receiver operating characteristic curve (area under the curve) of 0.71. This study confirmed a positive association between IgE concentration, eosinophil count and positive serology for T. canis. A general blood count, including eosinophils, is a simple test that can be performed in hospitals. Clinicians should target and screen for T.oxocara canis infection when children display clinical symptoms of itching, urticaria, erythema and eosinophilia. NCT05208333.

B-017 The Effect of Temperature on the Performance of Streptavidin-coated Paramagnetic Particles in Immunoassay Applications

Abstract Background Streptavidin-coated paramagnetic particles (streptavidin particles) are widely used in clinical immunoassays. Streptavidin has the highest affinity with biotin among all known non-covalent interaction we know today. With biotinylated molecules, be they small or large, strong binding of such molecules can be brought to streptavidin in a reliable and robust manner. In addition, streptavidin itself is a stable molecule, more resistant to heat, proteolysis, and chemical denaturation than a typical protein (1). Many publications illustrate the binding sites, binding forces, and configurations of streptavidin with or without biotin (2, 3). From our experience working with streptavidin particles in immunoassays, we know that the challenges to their applications are mainly with baseline signal, biotin interference, and thermal stability. This abstract describes our findings on the thermal stability of assay reagents made from streptavidin particles. Methods Intrigued by a recent publication that reports the effect of temperature on the affinity and stoichiometry of streptavidin with biotin (1), suggesting streptavidin’s binding capacity as a function of temperature in the range of 4°C to 40°C, we coupled streptavidin particles (Dynabeads T1 type) with biotinylated thyroxine hormone (T4), estradiol (E2), folate binding protein (FBP), and anti NT-proBNP antibody at varied temperatures between 4°C and 40°C, and then evaluated their coating capacity and thermal stability at 30°C or 37°C. The detection was alkaline phosphatase conjugates with anti T4 antibody, folate analogue, anti E2 antibody, and anti NT-proBNP antibody, respectively. The evaluation used Mindray’s automated chemiluminescent analyzer, CL6000i. Results Our data indicate that temperature plays a critical role in enhancing the performances of streptavidin particles in these immunoassays. From pre-coupling treatment of the particle to coupling with biotinylated ligands and subsequently post-coupling blocking and aging, temperature shows great impacts on the stability and tolerance to heat of the coupled particles at elevated temperatures. In contrast to the effectiveness of pre-coupling washing at 50°C or 55°C, coupling of streptavidin particles with biotinylated ligands favors a lower temperature, for example, ambient temperature and 4°C. Coupling at 37°C to 40°C results in slightly lower RLU signals in all four assays. Coupling at lower temperatures improves signal level and, more importantly, enhances thermal resistance of coupled particles. Post-coupling aging and optimization of diluent compositions can additionally improve accelerated stability data obtained at 37°C. Conclusion There are two mechanisms that negatively impact the stability performance of streptavidin particles coupled with ligands: One is gradual loss of loosely bound streptavidin molecules and the other streptavidin’s configurational and structural changes triggered by temperature changes. Both mechanisms can be countered by proper control of temperature in the multiple steps of making the solid phase reagents. Our findings can help immunoassay developers to design more robust assay reagents involving streptavidin particles.

AdvanTIG-202: A phase 2 study investigating anti-T cell immunoglobulin and ITIM domain monoclonal antibody ociperlimab plus tislelizumab in patients with previously treated recurrent or metastatic cervical cancer (333)

AdvanTIG-202: A phase 2 study investigating anti-T cell immunoglobulin and ITIM domain monoclonal antibody ociperlimab plus tislelizumab in patients with previously treated recurrent or metastatic cervical cancer (333)

Molecular Recognition of Surface Trans-Sialidases in Extracellular Vesicles of the Parasite Trypanosoma cruzi Using Atomic Force Microscopy (AFM).

Trans-sialidases (TS) are important constitutive macromolecules of the secretome present on the surface of Trypanosoma cruzi (T. cruzi) that play a central role as a virulence factor in Chagas disease. These enzymes have been related to infectivity, escape from immune surveillance and pathogenesis exhibited by this protozoan parasite. In this work, atomic force microscopy (AFM)-based single molecule-force spectroscopy is implemented as a suitable technique for the detection and location of functional TS on the surface of extracellular vesicles (EVs) released by tissue-culture cell-derived trypomastigotes (Ex-TcT). For that purpose, AFM cantilevers with functionalized tips bearing the anti-TS monoclonal antibody mAb 39 as a sense biomolecule are engineered using a covalent chemical ligation based on vinyl sulfonate click chemistry; a reliable, simple and efficient methodology for the molecular recognition of TS using the antibody-antigen interaction. Measurements of the breakdown forces between anti-TS mAb 39 antibodies and EVs performed to elucidate adhesion and forces involved in the recognition events demonstrate that EVs isolated from tissue-culture cell-derived trypomastigotes of T. cruzi are enriched in TS. Additionally, a mapping of the TS binding sites with submicrometer-scale resolution is provided. This work represents the first AFM-based molecular recognition study of Ex-TcT using an antibody-tethered AFM probe.

A recombinant monoclonal-based Taenia antigen assay that reflects disease activity in extra-parenchymal neurocysticercosis.

BackgroundAntigen tests for diagnosis and disease monitoring in some types of neurocysticercosis (NCC) are useful but access to testing has been limited by availability of proprietary reagents and/or kits.Methods/Principal findingsThree previously identified IgM-secreting hybridomas whose IgM products demonstrated specificity to Taenia solium underwent variable heavy and light chain sequencing and isotype conversion to mouse IgG. Screening of these recombinantly expressed IgG anti-Ts hybridomas, identified one (TsG10) with the highest affinity to crude Taenia antigen. TsG10 was then used as a capture antibody in a sandwich antigen detection immunoassay in combination with either a high titer polyclonal anti-Ts antibody or with biotinylated TsG10 (termed TsG10*bt). Using serum, plasma, and CSF samples from patients with active NCC and those from NCC-uninfected patients, ROC curve analyses demonstrated that the TsG10-TsG10-*bt assay achieved a 98% sensitivity and 100% specificity in detecting samples known to be antigen positive and outperformed the polyclonal based assay (sensitivity of 93% with 100% specificity). By comparing levels of Ts antigen (Ag) in paired CSF (n = 10) or plasma/serum (n = 19) samples from well-characterized patients with extra-parenchymal NCC early in infection and at the time of definitive cure, all but 2 (1 from CSF and 1 from plasma) became undetectable. There was a high degree of correlation (r = 0.98) between the Ag levels detected by this new assay and levels found by a commercial assay. Pilot studies indicate that this antigen can be detected in the urine of patients with active NCC.Conclusions/SignificanceA newly developed recombinant monoclonal antibody-based Ts Ag detection immunoassay is extremely sensitive in the detection of extra-parenchymal NCC and can be used to monitor the success of treatment in the CSF, serum/plasma and urine. The ability to produce recombinant TsG10 at scale should enable use of this antigen detection immunoassay wherever NCC is endemic.Clinical Trial RegistrationClinicalTrials.gov Identifiers: NCT00001205 - & NCT00001645.

Soroprevalência de Toxoplasma gondii em gatos domésticos na região tropical do Parque Estadual da Serra da Tiririca, Niterói, Rio de Janeiro

ABSTRACT The present study aimed to determine the seroprevalence of anti-T. gondii antibodies in cats of the Serra da Tiririca State Park region using the IFAT to evaluate the sex and age variables. The cats were domiciled in the region of Serra da Tiririca State Park (PESET-RJ), Rio de Janeiro. Between 2015 and 2016, a total of 86 blood samples were collected from 35 female and 51 male semi-domiciled cats that were attended to by a spay-neuter program of UFF. Samples were evaluated for anti-T. gondii immunoglobulin G by the indirect immunofluorescence reaction (IFAT) with a cut-off point of 1:40. Of the samples analyzed, 29.07% (25/86) presented anti-T gondii antibodies. There was no significant association (P> 0.05) between the variables sex and age of the animals with serology results. The results obtained in this study suggest that T. gondii has a considerable distribution among the cats of the studied region (PESET-RJ). This is the first report of the seroprevalence of T. gondii in cats from this area. Age and gender were not considered risk factors for infection by T. gondii in this group of animals studied.

Seroprevalence of Chagas disease in Southern Brazilian cardiac patients and their knowledge about the parasitosis and vectors.

Chagas disease (CD) is considered a typical low-income population sickness of the developing countries in Latin America. Given the historical relevance of CD in individuals in southern Rio Grande do Sul (RS) State, Brazil, the aim of this study was to identify the knowledge of the CD and its vectors by cardiac patients, and the prevalence of anti-T cruzi antibodies in these individuals in Pelotas, city located in Rio Grande do Sul (RS) state, Brazil. The subjects with cardiac disease were submitted to a semi-structured questionnaire as well as two serological tests in order to detect anti-T. cruzi IgG antibodies. Of the individuals that born in municipalities showing the highest triatomine infestation rates in recent decades, 81.8% were able to recognize the vector insect (p = 0.0042; OR = 5.9), and 83.3% reported either themselves or someone in their families to have CD (p = 0.043, OR = 5.2). Of the 54 patients submitted to serological analysis, only 01 patient (1.9%) was positive for anti-T. cruzi antibodies, a 55 year old man from the rural area of Canguçu county. This study provides support for the evaluation to be extended to other cardiology centers, given the importance of Chagas disease in Brazil.

The sea bass Dicentrarchus labrax as a marine model species in immunology: Insights from basic and applied research

This review summarizes the current knowledge on immune defence activities of the European sea bass Dicentrarchus labrax by reporting the consistent amount of work done on this economically-important species. A draft genome sequence is available for this species, together with whole transcriptomes from lymphoid and non-lymphoid tissues. Available full-length coding sequences of many immunoregulatory and immune-related genes allow for targeted quantitative PCR analysis, nowadays needed for -omics data verification, ex vivo and in vitro. The first anti-T cells monoclonal antibody teleost-wise was obtained in sea bass, followed by several monoclonal and polyclonal markers of lymphocyte populations, namely T cells (pan-T, CD3ε, TcRγ, CD45), and B cells (IgM, IgT, IgD). The combined use of molecular and biochemical tools enabled investigations on innate and acquired immune responses of sea bass in unstimulated/stimulated fish, along the development and under variable environmental conditions and food regimes. An overview of sea bass viral and bacterial pathogens and available vaccines against these microorganisms is also provided. The knowledge accumulated in the past 25 years validates the European sea bass as a reference marine model in the field of fish immunology.

Development of Polydiacetylene-Based Testosterone Detection as a Model Sensing Platform for Water-Insoluble Hormone Analytes

We have developed a polydiacetylene (PDA)-based sensing platform to detect testosterone (T) as a potential biomarker of preterm birth. The insolubility of the steroid hormone in water, where PDA assemblies are dispersed, poses a major issue, since they can hardly interact with each other. To overcome this challenge, acetonitrile was used as a suitable solvent. In addition, to minimize false signals of PDA assemblies caused by the solvent, a mixture of acetonitrile and distilled water was selected. To prove a concept of PDA-based sensing platform for targeting T hormone, we conjugated anti-T antibodies to surface of PDA assemblies to induce selective binding between T and anti-T antibodies. The fluorescence sensory signaling of the PDA-anti-T antibody conjugate was selectively generated for T, over 3.4 times higher sensitivity of the signaling compared to that from other sex steroid hormones studied (β-estradiol and progesterone).

Erythrocyte T-antigen activation in children: Patient characteristics and the hemolytic risk of transfusion.

T-antigen activation usually occurs upon red blood cell (RBC) membrane cryptantigen exposure due to bacterial enzymes. Although uncommon, the condition is probably underrecognized. There is concern about hemolysis after plasma and plasma-containing platelet transfusions due to naturally occurring anti-T antibody in healthy blood donors. However, experts have debated the extent and severity of clinical hemolysis due to anti-T. We retrospectively identified patients who tested positive for polyagglutination with Arachis hypogea and Glycine max lectins from 2008 to 2019. The records of the patients were reviewed to determine clinical symptoms, laboratory evidence of hemolysis, need for transfusion, and clinical outcomes. Ten patients were identified. At diagnosis, all were anemic and four had thrombocytopenia. Severe Streptococcus pneumoniae infection affected seven patients; one died. Seven of 10 patients (70%) had laboratory evidence of hemolysis. Peripheral blood smear findings in six patients included RBC agglutination and changes suggesting hemolysis (spherocytes and schistocytes), but three had unremarkable RBC morphology. Four patients required plasma or platelet transfusions; all survived to discharge. T-antigen activation is a rare entity. Most patients diagnosed at our hospital had hemolytic anemia and severe pneumococcal infection. Hemoglobin decreased after plasma and platelet transfusions in all patients assessed, but these transfusions were necessary to support treatment. RBCs were given to maintain appropriate hemoglobin levels.

Prevalência de anticorpos IgM e IgG anti-Toxoplasma gondii em universitários do Curso de Ciências Biológicas, Pontal do Triângulo Mineiro

Objetivo: Investigar a presença de IgG e IgM anti-Toxoplasma gondii no soro de estudantes de Ciências Biológicas da Universidade Federal de Uberlândia, campus do Pontal. Métodos: Estudo transversal de prevalência, com coleta de dados realizada entre junho de 2017 e fevereiro de 2018. Foram utilizadas as técnicas de Imunofluorescência Indireta e Ensaio Imunoenzimático (ELISA) e aplicados questionário semiestruturado para avaliação dos conhecimentos prévios sobre a toxoplasmose. Resultados: Participaram do estudo 128 alunos com faixa etária de 18 a 41 anos, sendo 83 (64,4%) do sexo feminino e 45 (35,6%) do sexo masculino. Foram colhidas amostras de sangue de 106 participantes e 13 (12,3%) apresentaram anticorpos anti-T. gondii. Destes, 3 (2,8%) afirmaram consumir leite bovino não pasteurizado, 3 (2,8%) carne crua ou mal passada e 1 (0,94%) vegetais crus ou não higienizados. Não foi observada associação estatisticamente significativa entre positividade (IgM anti-T. gondii e/ou IgG anti-T. gondii) e as variáveis analisadas no questionário.Conclusão: Neste trabalho foi possível verificar a presença de anticorpos IgM e IgG anti-T. gondii em universitários. Não se observou uma associação entre soropositividade e o hábito alimentar. Entretanto, a análise das respostas obtidas no questionário mostrou comportamento de risco por parte destes indivíduos, principalmente ao que se refere ao contato frequente com cães e gatos, muitas vezes recolhidos na rua.

Gold Nanoparticle Based Electrochemical Immunosensor for Detection of T3 Hormone.

We report a nanoparticles based electrochemical immunosensor to detect and quantify triiodothyronine (T3) hormone. Immunosensor developed using gold nanoparticles and anti-T3 antibody, was employed for quantification of T3 antigen using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) technique. The electrochemical response of the developed immunosensor correlates well with the amount of antigen present in the sample. With increase in antigen concentration the immunocomplex formation on electrode surface increases and hence redox current decreases. The immunosensor shows a lower limit of detection of 1 pg/mL and dynamic range from 1 to 500 pg/mL. Sensitivity of the immunosensor was found to be 29.81 μA/pg/mL/cm².

Immunohistochemical identification of T and B lymphocytes in formalin-fixed paraffin-embedded chicken tissues using commercial antibodies

Immunohistochemical method to detect avian lymphocytes is an efficient and reliable tool for accurate diagnosis, and immunological analysis of avian diseases. However, there are scarce studies reporting immunohistochemistry (IHC) using commercially available antibodies against lymphocytes in formalin-fixed paraffin-embedded (FFPE) chicken tissues. In the present study, we established an immunohistochemical method to identify chicken T and B lymphocytes in FFPE chicken tissues using commercial antibodies against chicken or human antigens. For this IHC method, the five tested anti-T lymphocyte antibodies reacted with chicken T lymphocytes on the FFPE sections. Further, 10 commercial anti-B lymphocyte antibodies were tested; of these, three successfully detected chicken B lymphocytes for IHC. In particular, anti-human CD3 (clone F7.2.38) antibody was most suitable for the detection of chicken T lymphocytes, whereas anti-chicken B cell activating factor receptor (BAFF-R) antibody (clone 2C4) was most suitable for the detection of chicken B lymphocytes under our IHC staining conditions. These two antibodies reacted with numerous lymphocytes of all representative lymphoid tissues without problematic background staining and nonspecific reactions. Our results indicate that T and B lymphocytes in FFPE chicken tissues can be immunohistochemically detected using commercial antibodies.

Quantitation of Thyroid Hormone Binding to Anti-Thyroxine Antibody Fab Fragment by Native Mass Spectrometry.

Thyroid hormones are important regulatory hormones, acting on nearly every cell in the body. The two main thyroid hormones are l-thyroxine (tetraiodo-l-thyronine, T4) and 3,3′,5-triiodo-l-thyronine (T3), which are produced in the thyroid gland and secreted into the blood stream. Other important thyroid hormone metabolites are 3,3′-diiodo-l-thyronine (T2) and l-thyronine (T0), which may show increased levels in circulation due to dietary iodine deficiency or other medical disorders. Owing to their central role in cellular functions, sensitive and specific detection methods for thyroid hormones are needed. In this work, native mass spectrometry (MS) was used to quantitate thyroid hormone binding to the anti-T4 antibody Fab fragment. First, the binding affinity for T2 was determined via direct ligand titration experiments. Then, the affinities for the other ligands were determined by competition experiments using T2 as the “low-affinity” reference ligand. The highest affinity was measured for T3, followed by T4, T2, and T0 (Kd = 29, 3.4, and 260 nM and 130 μM, respectively). Thus, it is evident that the number and positions of the iodine substituents within the thyronine rings are important for the ligand binding affinity of anti-T4 Fab. Surprisingly, structurally related tetrahalogen bisphenols were also able to bind to anti-T4 Fab with nanomolar affinities.

Investigation of a combination of amiodarone and itraconazole for treatment of American trypanosomiasis (Chagas disease) in dogs.

To evaluate clinical, serologic, parasitological, and histologic outcomes of dogs with naturally occurring Trypanosoma cruzi infection treated for 12 months with amiodarone and itraconazole. 121 dogs from southern Texas and southern Louisiana. Treatment group dogs (n = 105) received a combination of amiodarone hydrochloride (approx 7.5 mg/kg [3.4 mg/lb], PO, q 24 h, with or without a loading dosage protocol) and itraconazole (approx 10 mg/kg [4.5 mg/lb], PO, q 24 h, adjusted to maintain a plasma concentration of 1 to 2 μg/mL) for 12 months. Control group dogs (n = 16) received no antitrypanosomal medications. Serologic assays for anti-T cruzi antibodies, PCR assays for T cruzi DNA in blood, and physical evaluations were performed 1, 6, 9, 12, and 24 months after study initiation. Adverse events were recorded. Outcomes of interest were recorded and compared between groups. 86 of 105 treatment group dogs and 8 of 16 control group dogs survived and completed the study (5/19 and 6/7 deaths of treatment and control group dogs, respectively, were attributed to T cruzi infection). Mean survival time until death attributed to T cruzi was longer (23.19 vs 15.64 months) for the treatment group. Results of PCR assays were negative for all (n = 92) tested treatment group dogs (except for 1 dog at 1 time point) from 6 to 24 months after study initiation. Clinical improvement in ≥ 1 clinical sign was observed in 53 of 54 and 0 of 10 treatment and control group dogs, respectively; adverse drug events were minor and reversible. Results suggested efficacy of this trypanocidal drug combination for the treatment of T cruzi infection in dogs.

Toxoplasma infection in kidney donors and transplant recipients from Western Mexico: A one‐year follow‐up

Solid organ transplant recipients are highly susceptible to Toxoplasma gondii infection. We aimed to describe the 12-month follow-up risk of seroconversion in renal transplant recipients. Anti-Tgondii antibodies were investigated in donors and recipients of renal transplants. In donors, anti-Tgondii were evaluated before transplantation. In recipients, anti-Tgondii were monitored over a 12-month period to evaluate potential seroconversion or reactivation. IgG and IgM anti-T gondii antibodies were investigated through enzyme immunoassay and Western blot. Molecular diagnosis was performed on peripheral blood leukocytes using PCR to amplify fragments corresponding to the Tgondii B1 gene and the repetitive 529-bp element. The basal frequency of seropositive IgG anti-Tgondii antibodies was higher in donors than in recipients (38.4% vs 25.2%; P=.03). During the 12-month follow-up, the accumulated seroconversion to IgG and IgM antibodies was 3/99 (3.0%), and the accumulated reactivation was 11/99 (11.0%). None of the samples exhibited positivity to Tgondii DNA. This study showed that there is an increased risk of seroconversion or reactivation in renal transplant recipients over a 12-month follow-up. Our data suggest that prophylaxis with trimethoprim and sulfamethoxazole effectively prevented toxoplasmosis, since neither Tgondii DNA nor clinical toxoplasmosis was detected.

Purified human anti-Tn and anti-T antibodies specifically recognize carcinoma tissues

Described in several epithelial cancer cells, Tn- (GalNAcα1-O-Ser/Thr) and T- (Galβ3GalNAcα1-O-Ser/Thr) antigens are examples of tumor-associated antigens. Increased expression of Tn- and T-antigens is associated with tumor invasion and metastasis, and patients with high concentration of anti-Tn and anti-T antibodies have a more benign evolution of pathology. Asialofetuin (ASF) and ovine submaxillary mucin (OSM) are two glycoproteins that expose T- and Tn-antigen, respectively. In this work, using ASF or OSM we affinity-purified anti-T and anti-Tn antibodies from normal human plasma and tested their ability to specifically recognize tumor human tissues. Whereas purified anti-T antibodies (purity degree increase of 127-fold, and 22% recovery) were mainly IgG, for purified anti-Tn antibodies (purity degree enhancement of 125-fold, and 26% yield) the IgM fraction was predominant over the IgG one. IgG2 subclass was significantly enriched in both purified antibody samples. Purified antibodies did not bind normal human tissue (0/42), although recognized malignant tissues from different origin such as colon carcinoma (11/77 by anti-Tn; 7/79 by anti-T), breast carcinoma (10/23 by anti-Tn; 7/23 by anti-T), and kidney carcinoma (45/51 by anti-Tn; 42/51 by anti-T). Our results suggest that purified human anti-Tn and anti-T antibodies have a potential as anti-tumor therapeutic agents; restoring their levels in human sera could positively affect the evolution of patients with epithelial tumor pathologies.

MON-612 Familial Dysalbuminemic Hyperthyroxinemia Cases in Five Unrelated Japanese Families and the Influences on Free T4 Measurement

Familial dysalbuminemic hyperthyroxinemia (FDH) is caused by abnormal human serum albumin (HSA) with an increased thyroxine (T4) affinity leading to euthyroid hyperthyroxinemia. In Japanese FDH patients with the HSAR218P mutation, not only one-step but also two-step immunoassays for free T4 (FT4) can yield false-positive results. Therefore, it is difficult to distinguish FDH from syndrome of inappropriate secretion of TSH, even when multiple assays are used. Patient 1 was a 29-year-old pregnant woman. A radiographic examination and hormone stimulation test were not performed. We suspected that the patient had FDH because of her family history such as abnormal thyroid function and hyperthyroxinemia (Total T4 level was greater than the measurement sensitivity). Genetic analysis using direct sequencing for HSA revealed that she was consistent with FDH. She experienced a normal delivery. Other patients were performed the thyroid test with Chief complaints of infertility or depression and their thyroid function abnormalities were pointed out. Thyroid function tests revealed elevated FT4 and FT3 levels; their TSH level was within the reference range in all patients. To investigate T4 to HSA binding, gel filtration high-performance liquid chromatography was used for the biochemical analyses. Furthermore, FT4 was measured in FDH patients using one-step method LUMIPULSE (Fujirebio) using T3 as an antigen and an anti-T4 antibody as a label. The genomic analysis revealed a heterozygous missense mutation in HSA(R218P). In FDH patient sera, the albumin effluent corresponded to the peaks for total T4 (TT4); approximately 60% of the T4 in the effluent was detected as FT4. Mean FT4 level measured with LUMIPULSE was 1.28 ng/dL within the reference value range. In the FDH patients, a relatively larger quantity of T4 was bound to abnormal HSA. This bound T4 was measured as FT4 during the analysis. When thyroid function abnormality without clinical findings is observed, it is considered preferable to understand the antigen and antibody to be used and to select measurement method.

Association of Factors Involved in the Pathogenesis of Chagas Disease

Chagas disease, caused by the protozoan Trypanosoma cruzi, represents a serious health public problem with around seven million infected people worldwide. Approximately 30% of infected individuals will develop cardiac disorders during the chronic phase. However, the pathogenesis of Chagas disease remain incompletely elucidated with fundamental questions partially unanswered as the factors that lead to the development of clinical manifestations. Thereby, this study aims to investigate the importance of the association of T. cruzi strain, host sex, host immunological factors and changes in heart tissue in the progression of cardiac lesions in experimental Chagas disease. For this, 60 BALB/c mice were divided into three groups according to the T. cruzi strain (discrete typing unit TcI, TcII and TcVI). They were analyzed in acute phase (30 days pos‐infection ‐ 30dpi) and chronic phase (90 dpi). Ten uninfected mice formed the control group. Each group were formed by five males and five females. After the experimental period, mice were euthanized and blood and heart were collected. Anti‐T cruzi antibody and anti‐cardiac tissue antibody production were evaluated by ELISA. Parasite load in the heart was determined by qPCR. Histopathological analysis of heart was also performed. Most of the animals produced anti‐T. cruzi IgM antibody in the acute phase, whereas all mice were seropositive for IgG in chronic phase. TcI was characterized by elevated antibody levels with autoantibodies titers against the heart in chronic phase significantly higher than the other groups. Besides that TcI presented a greater number of parasites both in acute and chronic phase as well as more damage in heart tissue. No difference was observed between males and females. Amastigote nests were seen in mice analyzed in acute phase in TcI and TcVI, but not in TcII. The results confirm the participation of autoimmune response in chronic Chagas disease, which varies according to T. cruzi strain. It seems that the TcI was the most aggressive. However, the relationship between the studied factors and the severity of disease has not been established.Support or Funding InformationThis study was financed by Fundação de Apoio a Pesquisa do Distrito Federal (FAPDF), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES).This abstract is from the Experimental Biology 2019 Meeting. There is no full text article associated with this abstract published in The FASEB Journal.

Prevalence of antibody seroconversion to Toxoplasma gondii in uveitis and non-uveitis dogs

ObjectivesTo evaluate the prevalence of seroconversion to Toxoplasma gondii in dogs with uveitis and dogs without uveitis.MethodsIn total, 135 dogs were evaluated: 51 dogs were diagnosed with uveitis, and 84...