Production of baboon (papio hamadryas) monoclonal antibodies by herpesvirus papio immortalized baboon lymph node cells

1990 ◽  
Vol 126 (2) ◽  
pp. 287-294 ◽  
Author(s):  
R.M. Sharp ◽  
C.L. Durocher ◽  
J.L. Parmenter
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Wenbo Jiang ◽  
Julius Wong ◽  
Hyon-Xhi Tan ◽  
Hannah G. Kelly ◽  
Paul G. Whitney ◽  
...  

AbstractThe ferret is a key animal model for investigating the pathogenicity and transmissibility of important human viruses, and for the pre‐clinical assessment of vaccines. However, relatively little is known about the ferret immune system, due in part to a paucity of ferret‐reactive reagents. In particular, T follicular helper (Tfh) cells are critical in the generation of effective humoral responses in humans, mice and other animal models but to date it has not been possible to identify Tfh in ferrets. Here, we describe the screening and development of ferret-reactive BCL6, CXCR5 and PD-1 monoclonal antibodies. We found two commercial anti-BCL6 antibodies (clone K112-91 and clone IG191E/A8) had cross-reactivity with lymph node cells from influenza-infected ferrets. We next developed two murine monoclonal antibodies against ferret CXCR5 (clone feX5-C05) and PD-1 (clone fePD-CL1) using a single B cell PCR-based method. We were able to clearly identify Tfh cells in lymph nodes from influenza infected ferrets using these antibodies. The development of ferret Tfh marker antibodies and the identification of ferret Tfh cells will assist the evaluation of vaccine-induced Tfh responses in the ferret model and the design of novel vaccines against the infection of influenza and other viruses, including SARS-CoV2.


Immunology ◽  
1996 ◽  
Vol 87 (3) ◽  
pp. 447-453 ◽  
Author(s):  
M. HARADA ◽  
T. OKAMOTO ◽  
K. OMOTO ◽  
K. TAMADA ◽  
M. TAKENOYAMA ◽  
...  

1994 ◽  
Vol 40 (1) ◽  
pp. 49-61 ◽  
Author(s):  
David J. Hurley ◽  
Richard A. Wilson ◽  
Cynthia L. Baldwin ◽  
Jing-Yi Liu ◽  
Andrea M. Mastro

Blood ◽  
1985 ◽  
Vol 66 (5) ◽  
pp. 1017-1021 ◽  
Author(s):  
SL Giardina ◽  
RW Schroff ◽  
CS Woodhouse ◽  
DW Golde ◽  
RK Oldham ◽  
...  

Abstract Immunoglobulin gene rearrangement analysis and somatic cell hybridization techniques were used to examine the malignant cell population in an unusual patient with hairy cell leukemia and macroglobulinemia (N Engl J Med 296:92, 1977). Although previous investigations suggested that the IgM macroglobulin was secreted by the circulating leukemia cells, anti-idiotype monoclonal antibodies raised to the IgM macroglobulin failed to react with the malignant cells in the circulation and bone marrow. In contrast, approximately 50% of the mononuclear cells from an enlarged inguinal lymph node reacted strongly with the anti-idiotype antibodies. Subsequent reanalysis of all cell populations demonstrated that whereas the circulating and bone marrow cells were IgM kappa-bearing, the macroglobulin was IgM gamma-bearing and the lymph node cells were evenly divided among IgM kappa-bearing and IgM gamma-bearing. Immunofluorescence flow cytometry indicated that those lymph node cells that reacted strictly with the anti-idiotype antibody were IgM gamma-bearing, demonstrating that they were the source of macroglobulin. An analysis of immunoglobulin gene DNA confirmed the coexistence of two distinct malignant B cell populations in the lymph node and indicated that the IgM kappa-bearing lymph node cells were identical to the circulating and bone marrow leukemic cells.


Blood ◽  
1985 ◽  
Vol 66 (5) ◽  
pp. 1017-1021
Author(s):  
SL Giardina ◽  
RW Schroff ◽  
CS Woodhouse ◽  
DW Golde ◽  
RK Oldham ◽  
...  

Immunoglobulin gene rearrangement analysis and somatic cell hybridization techniques were used to examine the malignant cell population in an unusual patient with hairy cell leukemia and macroglobulinemia (N Engl J Med 296:92, 1977). Although previous investigations suggested that the IgM macroglobulin was secreted by the circulating leukemia cells, anti-idiotype monoclonal antibodies raised to the IgM macroglobulin failed to react with the malignant cells in the circulation and bone marrow. In contrast, approximately 50% of the mononuclear cells from an enlarged inguinal lymph node reacted strongly with the anti-idiotype antibodies. Subsequent reanalysis of all cell populations demonstrated that whereas the circulating and bone marrow cells were IgM kappa-bearing, the macroglobulin was IgM gamma-bearing and the lymph node cells were evenly divided among IgM kappa-bearing and IgM gamma-bearing. Immunofluorescence flow cytometry indicated that those lymph node cells that reacted strictly with the anti-idiotype antibody were IgM gamma-bearing, demonstrating that they were the source of macroglobulin. An analysis of immunoglobulin gene DNA confirmed the coexistence of two distinct malignant B cell populations in the lymph node and indicated that the IgM kappa-bearing lymph node cells were identical to the circulating and bone marrow leukemic cells.


1959 ◽  
Vol 234 (8) ◽  
pp. 1958-1965 ◽  
Author(s):  
Ernst Helmreich ◽  
Herman N. Eisen
Keyword(s):  

1967 ◽  
Vol 242 (13) ◽  
pp. 3242-3244
Author(s):  
Robert M. Swenson ◽  
Milton Kern
Keyword(s):  

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