1989
DOI: 10.1038/icb.1989.20
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Lymphocyte subpopulations in sheep during the early stage of experimental infection with bovine leukaemia virus

Abstract: Summary Stieep were experiraentalty infected with bovine leukaemia virus (BLV) by the inoculation of PBL from leukaemic sheep. Antibodies to viral structural proteins were detected at from 2 to 6 weeks after inoculation. At seroconversion, all sheep had a marked increase in the number of circulating lymphocytes, due essentially to an increase in the number of B cells. The number of circulating B cells then decreased but remained higher than pre-infection levels. A second increase in this population preceded th… Show more

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Cited by 13 publications
(8 citation statements)
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“…Together, these data demonstrate that primo-infection in sheep experimentally infected either with a wild type or mutant BLV proviruses is associated with a transient lymphocytosis, extending previous reports [11,12]. At seroconversion, all sheep exhibited a marked increase in the numbers of circulating B lymphocytes expressing for most of them the CD5 and CD11b cluster of differentiation markers and, interestingly, this phenomenon occurred independently of the type of mutant.…”
Section: Resultssupporting
confidence: 87%
“…Together, these data demonstrate that primo-infection in sheep experimentally infected either with a wild type or mutant BLV proviruses is associated with a transient lymphocytosis, extending previous reports [11,12]. At seroconversion, all sheep exhibited a marked increase in the numbers of circulating B lymphocytes expressing for most of them the CD5 and CD11b cluster of differentiation markers and, interestingly, this phenomenon occurred independently of the type of mutant.…”
Section: Resultssupporting
confidence: 87%
“…Blood-borne IgM ϩ cells, specifically IgM ϩ CD5 ϩ B cells (10), increase early during BLV infection of sheep and calves (11,29,50). The proliferation of IgM ϩ cells exceeds that for mock-infected controls and contributes to the increasing numbers of blood-borne B cells present at the time of seroconversion.…”
Section: Dissemination Of Infected Cells and Amplification Of Infectionmentioning
confidence: 99%
“…Suspensions of PBL in PBS containing 1% bovine serum albumin and 0-02% sodium azide (PBSA) were prepared by density gradient centrifugation from blood collected into EDTA, as described previously (11). A similar procedure was used to obtain lymphocyte suspensions from cell suspensions of lymph nodes, tumours and spleen, prepared by gently teasing the tissue samples in PBS and then filtering through gauze.…”
Section: Lymphocyte Suspensionsmentioning
confidence: 99%
“…After washing twice with PBSA the cells were resus-pended in 50 /iL of a predetermined optimal dilution of fluoroscein isothiocyanate (FITC)-conjugated-rabbit anti-mouse immunoglobulins (Dakopatts) and incubated at 4°C for 45 min. After washing twice with PBSA, the cells as resuspended in 30 /iL PBS containing 01% sodium azide and semi-permanent slides for epifluorescence microscopy were prepared, as described previously (11). In each preparation the percentage of labelled cells was determined by counting at least 200 lymphocytes.…”
Section: Monoclonal Antibodiesmentioning
confidence: 99%
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