Equine herpesvirus type 1 (EHV-1) is responsible for respiratory disorders, abortion and myeloencephalopathy (EHM) in horses. Two pathotypes of EHV-1 strains are circulating in the field: neurovirulent (N) and non-neurovirulent (NN). For both strains, CD172a+ monocytic cells are one of the main carrier cells of EHV-1 during primary infection, allowing the virus to invade the horse’s body. Recently, we showed that EHV-1 NN strains showed a restricted and delayed replication in CD172a+ cells. Here we characterize the in vitro replication kinetics of two EHV-1 N strains in CD172a+ cells and investigate if the replication of these strains is similarly silenced as shown for EHV-1 NN strains. We found that EHV-1 N replication was restricted to 7–8% in CD172a+ cells compared to 100% in control RK-13 cells. EHV-1 N replication was not delayed in CD172a+ cells but virus production was significant lower (103.0 TCID50/105 inoculated cells) than in RK-13 cells (108.5 TCID50/105 inoculated cells). Approximately 0.04% of CD172a+ cells produced and transmitted infectious EHV-1 to neighbour cells compared to 65% of RK-13 cells. Unlike what we observed for the NN strain, pretreatment of CD172a+ cells with histone deacetylases inhibitors (HDACi) did not influence the replication of EHV-1 N strains in these cells. Overall, these results show that the EHV-1 replication of N strains in CD172a+ cells differs from that observed for NN strains, which may contribute to their different pathogeneses in vivo. 相似文献
Chicks and chickens maintained under commercial conditions were vaccinated against Newcastle Disease via drinking water. Prior and after different times of vaccination blood samples were drawn from different numbers of birds and checked for HI antibodies. The modes of distribution of the antibody titers within the random sample were assayed. The following results were obtained:
1. 1. On the basis of the distribution of the serum titers can be concluded whether the antibody level within a flock is increasing or decreasing.
◦ —A right steep asymmetry can be observed up to 20 days post vaccination.
◦ —In the phase of maximal antibody levels an almost symmetric distribution of the titers is present.
◦ —In later times (more than three weeks p. vacc.) the distribution shows a left steep asymmetry (Poisson distribution).
2. 2. A poisson distribution is also observable during the elimination of maternal antibodies of chicks until complete elimination.
3. 3. The mode of distribution of the HI titers in sera of day-old chicks correlates with the mode of distribution of the dams. Therefore, conclusions are possible from the status of the chicks to the dams and reverse.
4. 4. Factors which interfere with the mode of distribution are:
◦ —Two or more peaks after vaccination of chickens. This indicates an uneven immune response within the flock.
◦ —Distributions with several peaks may also occur if flocks are composed of day-old chicks from parent flocks with different levels of antibody titers.
Résumé
Des poulets et des poussins maintenus dans un élevage conventionnel furent vaccinés contre la maladie de Newcastle par un vaccin administré dans l'eau de boisson. Avant et à différents temps après vaccination, des échantillons de sang furent prélevés sur un certain nombre de poussins et les anticorps inhibants de l'hémagglutination furent recherchés. Les modes de la distribution des titres en anticorps pour les échantillons pris au hasard furent recherchés. Les résultats suivants furent obtenus:
1. 1. Sur la base de la distribution des titres sériques, on peut conclure si le taux en anticorps à l'intérieur d'une population a augmenté ou diminué.
◦ —Une courbe asymétrique avec un pic déplacé vers la droite peut être observée 20 jours après la vaccination.
◦ —La phase correspondant au taux maximal en anticorps présente une distribution presque normale.
◦ —Plus tard, (au-delà de 3 semaines après la vaccination), la distribution apparaît asymétrique avec un déplacement vers la gauche (distribution de Poisson).
2. 2. Une distribution de Poisson peut aussi être observée au moment de l'élimination des anticorps d'origine maternelle chez des poussins jusqu'à complète élimination.
3. 3. Le mode de distribution des titres en anticorps inhibant l'hémagglutination dans des sérums de poussins d'un jour correspond au mode de distribution observé chez les mères. Des conclusions peuvent donc être faites à partir de l'état immunologique des poussins vis-à-vis des mères et viceversa.
4. 4. Les facteurs qui peuvent intervenir dans le mode de distribution sont:
◦ —Deux pics ou plus après la vaccination des poussins. Ceci indique qu'il existe une réponse immunitaire inégale dans la population.
◦ —Des distributions avec plusieurs pics peuvent être également observées si les populations sont composées de poussins de un jour provenant de populations parentales ayant des taux différents de titres en anticorps.
AIM: To confirm the existence of the endothelial progenitor cells in human cord blood and to study its differentiation and development process. METHODS: The mononuclear cells in human cord blood were isolated using lymphocyte separation solution. Then the mononuclear cells were cltured in MCDB131 containing 20% fetal bovine serum. The effects of 5 μmol/L dexamethasone, the extract from bovine brain, insulin and hypoxanine on the proliferation and differentiation of the adherent cells were observed. The morphology of the adherent cells were examined twice daily by inverted phase contrast microscope. CD34 and CD14 expression were determined by FACS. Immunohistochemistry was used to confirm the expression of factor Ⅷ. RESULTS: The proliferative endothelial progenitor cells existed within the CD34-adherent mononuclear cells of human cord blood. Dexamethasone and hypoxanine decreased the number of spindle-shaped cells and caudated cells. Bovine brain extract, insulin and FCS enhanced the number of spindle-shaped cells and caudated cells. CONCLUSION: The existence of endothelial progenitor cells within the CD34 - adherent monouclear cells of the human cord blood was observed and these cells were able to differentiate into endothelial-like cells in vitro. 相似文献
AIM: To investigate expression of CD44s in lung cancer and it's clinical significance. METHODS: A total of 117 primary lung cancer from patients were examined for CD44s expression by immunohistochemical staining. RESULTS: CD44s mostly expressed in non-small cell lung cancer (NSCLC) but not in small ecll lung cancer (SCLC), and squamous cell carcinoma(SCC) showed much stronger expression of CD44s than adenocarcinoma(ADC)(P<0.05). In comparison of the lung cancer with/ without lymph node metastasis, the latter showed stronger expression of CD44s(P<0.01). According to TNM, there was a distinct statistic difference between early stage and advanced stage(P<0.05). CONCLUSION: CD44s might be a better indicant in histological classification of lung cancer, lymph node metastasis, clinical stage and prognosis. 相似文献
AIM: To explore the ex vivo expansion characteristics of the endothelial progenitor cells (EPCs). METHODS: CD34+ cells were selected from umbilical cord blood mononuclear cells (MNC) by MiniMACS system, expanded at the same conditions as that for total MNC, coincubation of CD34+ and CD34- from the same donation for EPCs. In addition, we tested the effect of vessel endothelial growth factor (VEGF) and passage on cell differentiation, expansion kinetics and apoptosis. EPCs were determined and quantified by immunocytochemistry and flow cytometry. RESULTS: Coculture of CD34+ and CD34-,total MNC led to a significant increase in the expansion of CD34+ cells compared with CD34 enrichment (P<0.05). There was a trend toward decreased apoptosis in cultures when early passage was performed once the linear cord like structures appeared. There was no significant effect on apoptosis between with VEGF and without VEGF group (P>0.05). These differentiated EPCs were stained positive for CD34+, von Willebrand factor (vWF), KDR, CD31 and incorporate acetylated low-density lipoprotein (LDL). CD34+ and AC133+cells accounted for 68.2%±6.3% (n=6) and 57.2%±9.8% (n=6) of attaching (AT) cells at day 7 of culture, respectively. CONCLUSIONS: Coculture of CD34+ and CD34- or culture of MNC enhances ex vivo expansion of EPCs. Early passage decreases apoptosis rate, VEGF has no significant effect on ex vivo expansion of EPCs. 相似文献