Circulating Antigen-Antibody Complex Associated With Epstein-Barr Virus in Recurrent Burkitt's Lymphoma2

1973 ◽  
Vol 51 (4) ◽  
pp. 1319-1321 ◽  
Author(s):  
Tatsu Mukojima ◽  
Peter Gunvén ◽  
George Klein
Keyword(s):  
Epstein Barr Virus ◽  
Barr Virus ◽  
Circulating Antigen ◽  
Antibody Complex ◽  
Epstein Barr ◽  
Antigen Antibody

Immune Complexes Associated with Neoplasia: Presence of Epstein-Barr Virus Antigen-Antibody Complexes in Burkitt’s Lymphoma

Intervirology ◽  
1974 ◽  
Vol 4 (5) ◽  
pp. 292-302 ◽  
Author(s):  
Michael B.A. Oldstone ◽  
Argyrios N. Theofilopoulos ◽  
Peter Gunvén ◽  
George Klein
Keyword(s):  
Immune Complexes ◽  
Epstein Barr Virus ◽  
Burkitt’S Lymphoma ◽  
Virus Antigen ◽  
Burkitt's Lymphoma ◽  
Barr Virus ◽  
Epstein Barr ◽  
Antigen Antibody

COMPLEXITY OF ANTIGEN-ANTIBODY SYSTEMS ASSOCIATED WITH EPSTEIN-BARR VIRUS

1971 ◽  
Vol 177 (1 Defined Immun) ◽  
pp. 241-249 ◽  
Author(s):  
Arne Svedmyr ◽  
Aberra Demissie ◽  
George Klein ◽  
Lajos Gergely ◽  
Peter Clifford
Keyword(s):  
Epstein Barr Virus ◽  
Barr Virus ◽  
Epstein Barr ◽  
Antigen Antibody

scholarly journals Strong Correlations of Anti–Viral Capsid Antigen Antibody Levels in First‐Degree Relatives from Families with Epstein‐Barr Virus–Related Lymphomas

2009 ◽  
Vol 199 (8) ◽  
pp. 1121-1127 ◽  
Author(s):  
Caroline Besson ◽  
Corinne Amiel ◽  
Catherine Le‐Pendeven ◽  
Sabine Plancoulaine ◽  
Colette Bonnardel ◽  
...  
Keyword(s):  
Epstein Barr Virus ◽  
Viral Capsid ◽  
Viral Capsid Antigen ◽  
Strong Correlations ◽  
Barr Virus ◽  
First Degree Relatives ◽  
Epstein Barr ◽  
Antigen Antibody ◽  
Antibody Levels

A Quantitative Ultrastructural Study of Peripheral Blood Lymphocytes Containing Parallel Tubular Arrays in Epstein-Barr Virus and Cytomegalo-Virus Mononucleosis

1981 ◽  
Vol 39 ◽  
pp. 454-455
Author(s):  
C. M. Payne ◽  
P. M. Tennican
Keyword(s):  
Peripheral Blood ◽  
Lymphocyte Count ◽  
Epstein Barr Virus ◽  
Absolute Lymphocyte Count ◽  
Peripheral Blood Lymphocytes ◽  
Clinical State ◽  
Barr Virus ◽  
The Absolute ◽  
Epstein Barr ◽  
Tubular Arrays

In the normal peripheral circulation there exists a sub-population of lymphocytes which is ultrastructurally distinct. This lymphocyte is identified under the electron microscope by the presence of cytoplasmic microtubular-like inclusions called parallel tubular arrays (PTA) (Figure 1), and contains Fc-receptors for cytophilic antibody. In this study, lymphocytes containing PTA (PTA-lymphocytes) were quantitated from serial peripheral blood specimens obtained from two patients with Epstein -Barr Virus mononucleosis and two patients with cytomegalovirus mononucleosis. This data was then correlated with the clinical state of the patient.It was determined that both the percentage and absolute number of PTA- lymphocytes was highest during the acute phase of the illness. In follow-up specimens, three of the four patients' absolute lymphocyte count fell to within normal limits before the absolute PTA-lymphocyte count.In one patient who was followed for almost a year, the absolute PTA- lymphocyte count was consistently elevated (Figure 2). The estimation of absolute PTA-lymphocyte counts was determined to be valid after a morphometric analysis of the cellular areas occupied by PTA during the acute and convalescent phases of the disease revealed no statistical differences.

Studies of Epstein-Barr Virus Antigens Using Immunoperoxidase and Immunofluorescence Techniques

1975 ◽  
Vol 33 ◽  
pp. 342-343
Author(s):  
R. Stephens ◽  
K. Traul ◽  
D. Woolf ◽  
P. Gaudreau
Keyword(s):  
Electron Microscopy ◽  
Nasopharyngeal Carcinoma ◽  
Epstein Barr Virus ◽  
Barr Virus ◽  
If Technique ◽  
Infected Cells ◽  
Virus Antigens ◽  
Epstein Barr ◽  
Virus Capsid Antigen ◽  
Antigen Reactivity

A number of antigens have been found associated with persistent EBV infections of lymphoblastoid cells. Identification and localization of these antigens were principally by immunofluorescence (IF) techniques using sera from patients with nasopharyngeal carcinoma (NPC), Burkitt lymphoma (BL), and infectious mononucleosis (IM). Our study was mainly with three of the EBV related antigens, a) virus capsid antigen (VCA), b) membrane antigen (MA), and c) early antigens (EA) using immunoperoxidase (IP) techniques with electron microscopy (EM) to elucidate the sites of reactivity with EBV and EBV infected cells.Prior to labeling with horseradish peroxidase (HRP), sera from NPC, IM, and BL cases were characterized for various reactivities by the indirect IF technique. Modifications of the direct IP procedure described by Shabo and the indirect IP procedure of Leduc were made to enhance penetration of the cells and preservation of antigen reactivity.

Quantitative analysis of circulating cell-free Epstein-Barr virus (EBV) DNA levels in patients with EBV-associated lymphoid malignancies

2000 ◽  
Vol 111 (1) ◽  
pp. 239-246 ◽  
Author(s):  
Kenny I. K. Lei ◽  
Lisa Y.S. Chan ◽  
Wing Y. Chan ◽  
Philip J. Johnson ◽  
Y. M. Dennis Lo
Keyword(s):  
Quantitative Analysis ◽  
Epstein Barr Virus ◽  
Barr Virus ◽  
Lymphoid Malignancies ◽  
Ebv Dna ◽  
Epstein Barr

Chronic bullous disease of childhood following Epstein-Barr virus seroconversion: a case report

1996 ◽  
Vol 21 (2) ◽  
pp. 123-126
Author(s):  
U. BALDARI ◽  
A. ASCARI RACCAGNI ◽  
B. CELLI ◽  
M. GIOVANNA RIGHINI
Keyword(s):  
Case Report ◽  
Epstein Barr Virus ◽  
Barr Virus ◽  
Bullous Disease ◽  
Epstein Barr
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