Further Studies on Interactions Between Graft Reactions Sessile and Humoral Antibodies in Homo-Graft Reactions

Author(s):  
J. R. Batchelor ◽  
M. S. Silverman
Keyword(s):  
JAMA ◽  
1966 ◽  
Vol 198 (3) ◽  
pp. 226-230 ◽  
Author(s):  
F. Milgrom

Pharmaceutics ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 281
Author(s):  
Isaías Sanmartín ◽  
Luis Sendra ◽  
Inés Moret ◽  
María José Herrero ◽  
Salvador F. Aliño

Vector design and its characterization is an area of great interest in current vaccine research. In this article, we have formulated and characterized a multicompartmental lipopolyplex, which associates multiple liposomes and polyplexes in the same complex. These particles allow the simultaneous delivery of lipid or water-soluble antigens associated with genes to the same cell, in much higher amounts than conventional lipopolyplexes. The vector characterization and optimization were carried out using liposomes with entrapped carboxyfluorescein and adapted electrophoretic assays. Two types of lipopolyplexes (containing hydrophilic or lipophilic antigens) were employed to evaluate their interest in vaccination. The lipopolyplex loaded with an extract of water-soluble melanoma proteins proved to efficiently induce humoral response in murine melanoma model, increasing the levels of IgM and IgG. The specificity of the immune response induced by the lipopolyplex was demonstrated in mice with the lipopolyplex containing the GD3 ganglioside lipid antigen, abundant in melanoma cells. The levels of anti-GD3 IgG increased markedly without modifying the expression of humoral antibodies against other gangliosides.


1979 ◽  
Vol 13 (1) ◽  
pp. 77-78
Author(s):  
L. Pávková ◽  
Z. Koničková ◽  
R. Königová ◽  
R. Vrabec

Biomolecules ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 868 ◽  
Author(s):  
Khan M. A. Hassan ◽  
John D. Hansen ◽  
Brantley R. Herrin ◽  
Chris T. Amemiya

The variable lymphocyte receptors (VLRs) consist of leucine rich repeats (LRRs) and comprise the humoral antibodies produced by lampreys and hagfishes. The diversity of the molecules is generated by stepwise genomic rearrangements of LRR cassettes dispersed throughout the VLRB locus. Previously, target-specific monovalent VLRB antibodies were isolated from sea lamprey larvae after immunization with model antigens. Further, the cloned VLR cDNAs from activated lamprey leukocytes were transfected into human cell lines or yeast to select best binders. Here, we expand on the overall utility of the VLRB technology by introducing it into a filamentous phage display system. We first tested the efficacy of isolating phage into which known VLRB molecules were cloned after a series of dilutions. These experiments showed that targeted VLRB clones could easily be recovered even after extensive dilutions (1 to 109). We further utilized the system to isolate target-specific “lampribodies” from phage display libraries from immunized animals and observed an amplification of binders with relative high affinities by competitive binding. The lampribodies can be individually purified and ostensibly utilized for applications for which conventional monoclonal antibodies are employed.


1970 ◽  
Vol 282 (3) ◽  
pp. 111-117 ◽  
Author(s):  
M. Jeannet ◽  
V. W. Pinn ◽  
M. H. Flax ◽  
H. J. Winn ◽  
P. S. Russell
Keyword(s):  

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