The efforts for the development and testing of vaccines against Trypanosoma cruzi infection have increased during the past years. We have designed a TcVac series of vaccines composed of T. cruzi derived, GPI-anchored membrane antigens. The TcVac vaccines have been shown to elicit humoral and cellular mediated immune responses and provide significant (but not complete) control of experimental infection in mice and dogs. Herein, we aimed to test two immunization protocols for the delivery of DNA-prime/DNA-boost vaccine (TcVac1) composed of TcG2 and TcG4 antigens in a BALB/c mouse model. Mice were immunized with TcVac1 through intradermal/electroporation (IDE) or intramuscular (IM) routes, challenged with T. cruzi, and evaluated during acute phase of infection. The humoral immune response was evaluated through the assessment of anti-TcG2 and anti-TcG4 IgG subtypes by using an ELISA. Cellular immune response was assessed through a lymphocyte proliferation assay. Finally, clinical and morphopathological aspects were evaluated for all experimental animals. Our results demonstrated that when comparing TcVac1 IDE delivery vs IM delivery, the former induced significantly higher level of antigen-specific antibody response (IgG2a + IgG2b > IgG1) and lymphocyte proliferation, which expanded in response to challenge infection. Histological evaluation after challenge infection showed infiltration of inflammatory cells (macrophages and lymphocytes) in the heart and skeletal tissue of all infected mice. However, the largest increase in inflammatory infiltrate was observed in TcVac1_IDE/Tc mice when compared with TcVac1_IM/Tc or non-vaccinated/infected mice. The extent of tissue inflammatory infiltrate was directly associated with the control of tissue amastigote nests in vaccinated/infected (vs. non-vaccinated/infected) mice. Our results suggest that IDE delivery improves the protective efficacy of TcVac1 vaccine against T. cruzi infection in mice when compared with IM delivery of the vaccine.

Background: Several efforts have been made to improve the glass ionomer cements (GICs) properties with nanotechnology. Fluoride release in once of most beneficial properties of GICs. The purpose of this study was to evaluate the fluoride release, recharge, and cytotoxicity in GICs reinforced with titanium dioxide nanoparticles (TiO₂N). Objective: Evaluate the fluoride release, recharge, and cytotoxicity in GICs reinforced with TiO₂N. Methods: Four GICs, FUJI IX EXTRA (G1c), KETAC MOLAR (G2c), IONOFILL MOLAR (G3c), and FUJI IX (G4c) were combined with TiO₂N (G1e, G2e, G3e, and G4e) and divided into blocks of 5-mm width and 1-mm thickness 10 each. A total of 80 samples were arranged as follows: GICs alone as negative control (n = 40) and GICs + TiO₂N as experimental groups (n = 40). The fluoride release was determined for periods of 1, 2, 6, 10, 31, 90, 180, 240, and 300 days. On days 30 and 179, samples were recharged by submerging in 1 mL of 20,000 ppm sodium fluoride gel. Cytotoxic activity was carried out with gingival fibroblasts, using 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide cell viability assay. Results: The experimental groups obtained the highest and more constant fluoride released when compared to control groups. After the first recharge, experimental groups (G1e, G3e, and G4e) showed statistically significant results (P = .001, 0.010, and 0.001 respectively) enhancing their recharge ability regarding control groups. The second recharge showed better results in G1e concerning the rest of the groups. No cytotoxic activity was observed in all experimental groups, although significant differences were observed in G3e and G4e regarding control group. Conclusion: The incorporation of TiO₂N enhance the fluoride release in glass ionomers with a noncytotoxic effect on human gingival fibroblasts.

Ticks are a problem for cattle production mainly in tropical and subtropical regions, because they generate great economic losses. Acaricides and vaccines have been used to try to keep tick populations under control. This has been proven difficult given the resistance to acaricides and vaccines observed in ticks. Resistance to protein rBm86-based vaccines has been associated with the genetic diversity of Bm86 among the ectoparasite’s populations. So far, neither genetic diversity, nor spatial distribution of circulating Bm86 haplotypes, have been studied within the Mexican territory. Here, we explored the genetic diversity of 125 Bm86 cDNA gene sequences from R. microplus from 10 endemic areas of Mexico by analyzing haplotype distribution patterns to help in understanding the population genetic structure of Mexican ticks. Our results showed an average nucleotide identity among the Mexican isolates of 98.3%, ranging from 91.1 to 100%. Divergence between the Mexican and Yeerongpilly (the Bm86 reference vaccine antigen) sequences ranged from 3.1 to 7.4%. Based on the geographic distribution of Bm86 haplotypes in Mexico, our results suggest gene flow occurrence within different regions of the Mexican territory, and even the USA. The polymorphism of Bm86 found in the populations included in this study, could account for the poor efficacy of the current Bm86 antigen based commercial vaccine in many regions of Mexico. Our data may contribute towards designing new, highly-specific, Bm86 antigen vaccine candidates against R. microplus circulating in Mexico.

The discrepancy index evaluates the complexity of the initial orthodontic diagnosis. The objective is to compare whether there is a difference in the final discrepancy index score of the American Board of Orthodontics (ABO) when obtained using digital and manual techniques. Fifty-six initial orthodontic records in a digital and physical format were included (28 each) in 2022 at the Center for Research and Advanced Studies in Dentistry. For the digital measurements, iTero and TRIOS 3 intraoral scanners were used, along with Insignia software and cephalometric tracing with Dolphin Imaging software. Manual measurements were obtained in dental casts using the ruler indicated for the previously mentioned discrepancy index, in addition to conventional cephalometric tracing. Student’s t-test did not show statistically significant differences between the digital and manual techniques, with final discrepancy index scores of 24.61 (13.34) and 24.86 (14.14), respectively (p = 0.769). Cohen’s kappa index showed very good agreement between both categorical measurements (kappa value = 1.00, p = 0.001). The Bland–Altman method demonstrated a good agreement between continuous measurements obtained by both techniques with a bias of 0.2500 (superior limit of agreement =9.0092988, inferior limit of agreement = −8.5092988). Excellent agreement was observed in obtaining the discrepancy index through digital technique (Intraoral scanning and digital records) and manual technique (conventional records).

Objective: Our objective was to determine the salivary levels of cobalt, nickel, chromium, and titanium ions at the end of fixed orthodontic treatment and during the post-removal period (1 and 3 months after removal of the fixed appliance). Methods: This pilot longitudinal study included fifteen individuals (10 females and 5 males). Five milliliters of saliva was collected at three time points: T1 (before withdrawal of orthodontic appliances), T2 (one month post-withdrawal), and T3 (three months post-withdrawal). The concentrations of nickel (Ni), titanium (Ti), chromium (Cr), and cobalt (Co) in the samples were analyzed using Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). All samples were analyzed in triplicate. The data were analyzed by repeated-measures ANOVA, and differences were considered significant if the p-value was ≤0.05. Results: The concentrations of Co, Cr, and Ti at the three time points were low and decreased after the removal of the orthodontic appliance, while Ni showed an increase at T3. Co and Ni showed significant differences between T3 and T1 (p = 0.016 and p = 0.029, respectively). There was also significantly increased Ni ion release at T3 compared to T2 (p = 0.010). The Cr and Ti levels at all three time points were significantly different (Cr: p = 0.001; Ti: p = 0.001 and p = 0.005). Conclusions: The levels of cobalt, chromium, and titanium in saliva decreased after removal of the orthodontic appliance, whereas nickel increased at T3. However, the levels were below the mean dietary intake levels; therefore, these concentrations can be considered non-toxic. This study has limitations that should be considered when interpreting the results.

Aim: The aim of the present study is to determine the reliability of the lateral cephalometric radiography and orthopantomography in the diagnosis of skeletal maturation for nine to eighteen years old subjects in two populations. Materials and methods: A cross-sectional study was performed with a sample of 72 patient records from the Orthodontics Departments at the Autonomous University of Yucatan (southeast of Mexico) and the Autonomous University of the State of Mexico (central Mexico). Patients aged between 9 and 18 years old.Samples were divided into six groups (36 radiographs/group). Groups I and IV were analyzed with Björk, Grave, and Brown’s systems, groups II and V with Hassel and Farman methods, and groups III and VI with the Demirjian Index. The degree of intra-observer agreement between all methods of predicting skeletal maturation was measured using the weighted kappa statistics. The correlation between the hand-wrist analysis, cervical vertebrae maturation, and the stages of mandibular second molar was evaluated by the Spearman correlation method. Results: The kappa coefficient was 0.919 for hand-wrist analysis, while 0.839 and 0.915 for cervical vertebrae maturation and dental age, respectively. Spearman’s (r) correlation values were between GI and GII r = 0.900, GI and GIII r = 0.823, GII and GIII r = 0.826, GIV and GV r = 0.893, GIV and GVI r = 0.862, GV and GVI r = 0.843 with P ≤ 0.05. Conclusion: Lateral cephalometric radiography and orthopantomography is effective in determining skeletal maturation.