ABSTRACT
O objetivo do presente estudo foi avaliar a correlação entre a contagem automática de células somáticas (CCS) com a porcentagem de neutrófilos pela técnica de citocentrifugação e pela citometria de fluxo. Para tal, 102 amostras de leite proveniente de 28 vacas da raça Holandesa foram coletadas e submetidas ao isolamento de células do leite e posterior identificação da população de neutrófilos. Após citocentrifugação, os neutrófilos foram identificados por microscopia óptica utilizando-se o corante de Rosenfeld. Os neutrófilos lácteos foram identificados por citometria de fluxo utilizando anticorpo monoclonal específico (CH138A) e anticorpo monoclonal secundário conjugado à ficoeritrina. O presente estudo demonstrou correlação positiva entre a CCS e a porcentagem de neutrófilos por citometria de fluxo (r= 0,625) e pela técnica de citocentrifugação (r= 0,267). Observou-se também correlação positiva entre a porcentagem de neutrófilos pela citometria de fluxo e pela técnica de citocentrifugação (r = 0,496), embora a porcentagem de neutrófilos no leite tenha sido maior pela técnica de citocentrifugação quando comparada com a citometria de fluxo. Deste modo, o presente estudo indica que a citometria de fluxo pode ser uma ferramenta útil no diagnóstico e controle da mastite bovina.
The purpose of the present study was to assess the correlation between the automatic somatic cell count (SCC) and the percentage of neutrophils through cytocentrifugation technique and flow cytometry. Thus, 102 milk samples from 28 Holstein dairy cows were collected and submitted to milk cell isolation procedures, and afterwards, the neutrophils were identified. After cytocentrigugation, the neutrophils were microscopically identified using the rosenfeld dye. The milk neutrophils were recognized by flow cytometry using primary mouse IgM monoclonal antibody (CH138A) and phycoerytrin (PE) goat anti-mouse IgM antibody. This study found a positive correlation between SCC and the percentage of neutrophils through cytocentrifugation (r= 0.267) and flow cytometry (r= 0.625). A positive correlation was also encountered between the percentage of neutrophils through cytocentrifugation and flow cytometry (r= 0.496), although the percentage of neutrophils was higher in samples submitted to cytocentrifugation. In conclusion, flow cytometry can be a useful tool in the diagnosis and control of mastitis.
Subject(s)
Animals , Female , Cattle , Flow Cytometry/veterinary , Mastitis, Bovine , Neutrophils/cytologyABSTRACT
BACKGROUND: This study was purposed to find out the differences in the lymphocyte subsets and differential cell counts of the bronchoalveolar lavage (BAL) fluid in patients with interstitial lung disease (ILD) and to analyze the differences according to their ages, gender and smoking habits. METHODS: BAL fluid samples of 141 ILD patients were examined for lymphocyte subsets and differential cell counts, and the differences among the patients were analyzed according to their diseases. Then, within the three most common disease groups, the differences were further analyzed by the age, gender and smoking habit of the patients. RESULTS: There were no statistically significant differences in total cell counts (per millimeters of BAL fluid) among the patient groups with each ILD. However, significant differences were observed in the percentages of neutrophils, lymphocytes, eosinophils, and macrophages of BAL fluid. Also, in lymphocyte subset analyses, the percentages of total T cells, B cells, CD4+ T cells, CD8+ T cells, CD4/CD8 T cell ratios, and NK cells were significantly different among the patients with each ILD. However, within the same disease group, there were no differences in differential cell counts and lymphocyte subset analyses according to the age, smoking habit, and gender of the patients. CONCLUSIONS: Although the age, smoking habit and gender did not have an effect on the BAL fluid analyses among the patients with the same ILD, there were significant differences among the patients with each ILD; therefore, the differential cell counts and lymphocyte subset analyses of BAL fluid can be useful in differential diagnosis for determining the types of ILD.
Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Bronchoalveolar Lavage Fluid/cytology , Diagnosis, Differential , Lung Diseases, Interstitial/diagnosis , Lymphocyte Count , Lymphocyte Subsets/immunology , SmokingABSTRACT
BACKGROUND: The total and differential cell count of bronchoalveolar lavage(BAL) fluid are useful assessing activity, prognosis and response to therapy in diffuse interstitial lung disease. But controversy exist as to the appropriate method in processing BAL fluid. Therefore we investigated the effect of gauze filtration, centrifugation and different storage time of BAL fluid on the total and differential cell count. METHOD: We obtained BAL fluid from 6 persons with no active lung lesion and divided pooled BAL fluid into several siliconized glass tubes and filtered through 0,1, 2, 4 folds of cotton guaze(pore size:lmm), and compared total cell count using hemocytometer after trypan blue staining and differential cell count after Wright-Giemsa staining of cytocentrifuged preparations. And we also counted total and differential cell count after centrifugation(400g for 30 mm) and various storage time(2hr, 24hr, and 48hr). RESULTS: There was no difference in total and differential cell count according to folds of gauze filtraion. But without gauze filtration, mucus threads that hampered total and differential cell count were found in 2 cases (33%). Centrifugation resulted in loss of total cell count(24+/-18%) without change in differential cell count. There was no change in total cell count after 21w storage but significant cell loss was found after 241w storage time(24hr : 28+/-21%, 48hr: 41+/-24%). However there was no change in differential cell count with 48hr storage time. CONCLUSION: Total and differential cell count of BAL fluid may be best performed after cotton gauze filtration without centrifugation and within 2 hours.