Skip to main content
Immunology logoLink to Immunology
. 1971 Oct;21(4):583–594.

Structural control of immunogenicity

II. Antibody synthesis and cellular immunity in response to immunization with mono-ε-oligo-L-lysines*

Yehudit Stupp, W E Paul, B Benacerraf
PMCID: PMC1408242  PMID: 5121756

Abstract

A detailed evaluation of the capacity of mono-ε-DNP-oligo-L-lysines to initiate anti-DNP antibody synthesis and a state of delayed hypersensitivity in guinea-pigs is presented. Peptides containing as few as two lysine residues elicit the production of significant amounts of anti-DNP antibody when they are administered as Freund's complete adjuvant emulsions. Under these immunization conditions, the serum concentration of anti-DNP antibody is dependent on the chain length of the peptide, and on the amount and kind of mycobacteria in the adjuvant; guinea-pigs lacking the PLL gene produce amounts of anti-DNP antibody indistinguishable from that produced by guinea-pigs possessing this gene. On the other hand, when guinea-pigs are immunized with either 1-ε-DNP-tetra-L-lysine or 1-ε-DNP-nona-L-lysine without the use of mycobacterial adjuvant, anti-DNP antibody is produced only by guinea-pigs receiving the nona-L-lysine and only by those animals possessing the PLL gene.

Delayed hypersensitivity results from immunizing PLL+ guinea-pigs with mono-ε-DNP-octa and nona-lysines but not from immunization with mono-ε-DNP-hexa-lysine; PLL— animals do not exhibit delayed hypersensitivity to any of these compounds.

The data suggest that antibody synthesis to positively charged compounds may proceed as a result of formation of charge complexes with mycobacterial proteins; under such immunization conditions the intrinsic immunogenicity of a compound is more reliably revealed by the induction or elicitation of cellular immune responses. On this basis, a definite discontinuity in the degree of immunogenicity of the mono-ε-DNP-oligo-L-lysines occurs as the peptides are lengthened from six to eight residues.

Full text

PDF
583

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BENACERRAF B., LEVINE B. B. Immunological specificity of delayed and immediate hypersensitivity reactions. J Exp Med. 1962 May 1;115:1023–1036. doi: 10.1084/jem.115.5.1023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. FARR R. S. A quantitative immunochemical measure of the primary interaction between I BSA and antibody. J Infect Dis. 1958 Nov-Dec;103(3):239–262. doi: 10.1093/infdis/103.3.239. [DOI] [PubMed] [Google Scholar]
  3. FREUND J. The mode of action of immunologic adjuvants. Bibl Tuberc. 1956;(10):130–148. [PubMed] [Google Scholar]
  4. Green I., Benacerraf B., Stone S. H. The effect of the amount of mycobacterial adjuvants on the immune response of strain 2, strain 13 and Hartley strain guinea pigs to DNP-PLL and DNP-GL. J Immunol. 1969 Sep;103(3):403–412. [PubMed] [Google Scholar]
  5. Green I., Paul W. E., Benacerraf B. Genetic control of immunological responsiveness in guinea pigs to 2,4-dinitrophenyl conjugates of poly-L-arginine, protamine, and poly-L-ornithine. Proc Natl Acad Sci U S A. 1969 Nov;64(3):1095–1102. doi: 10.1073/pnas.64.3.1095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Green I., Paul W. E., Benacerraf B. The behavior of hapten-poly-L-lysine conjugates as complete antigens in genetic responder and as haptens in nonresponder guinea pigs. J Exp Med. 1966 May 1;123(5):859–879. doi: 10.1084/jem.123.5.859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. KANTOR F. S., OJEDA A., BENCARERRAF B. Studies on artifical antigens. I. Antigenicity of DNP-polylysine and DNP copolymer of lysine and glutamic acid in guinea pigs. J Exp Med. 1963 Jan 1;117:55–69. doi: 10.1084/jem.117.1.55. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LEVINE B. B., OJEDA A., BENACERRAF B. STUDIES ON ARTIFICIAL ANTIGENS. III. THE GENETIC CONTROL OF THE IMMUNE RESPONSE TO HAPTEN-POLY-L-LYSINE CONJUGATES IN GUINEA PIGS. J Exp Med. 1963 Dec 1;118:953–957. doi: 10.1084/jem.118.6.953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. PLESCIA O. J., BRAUN W., PALCZUK N. C. PRODUCTION OF ANTIBODIES TO DENATURED DEOXYRIBONUCLEIC ACID (DNA). Proc Natl Acad Sci U S A. 1964 Aug;52:279–285. doi: 10.1073/pnas.52.2.279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Paul W. E., Kask A. M. Structural control of immunogenicity. I. Synthesis of oligo-L-lysine peptides and their mono-epsilon-DNP derivatives. Immunology. 1971 Oct;21(4):575–582. [PMC free article] [PubMed] [Google Scholar]
  11. Paul W. E., Stupp Y., Siskind G. W., Benacerraf B. Structural control of immunogenicity. IV. Relative specificity of elicitation of cellular immune responses and of ligand binding to anti-hapten antibody after immunization with mono-epsilon-DNP-nona-L-lysine. Immunology. 1971 Oct;21(4):605–616. [PMC free article] [PubMed] [Google Scholar]
  12. Schlossman S. F., Ben-Efraim S., Yaron A., Sober H. A. Immunochemical studies on the antigenic determinants required to elicit delayed and immediate hypersensitivity reactions. J Exp Med. 1966 Jun 1;123(6):1083–1095. doi: 10.1084/jem.123.6.1083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Schlossman S. F., Yaron A., Ben-Efraim S., Sober H. A. Immunogenicity of a series of alpha,N-DNP-L-lysines. Biochemistry. 1965 Aug;4(8):1638–1645. doi: 10.1021/bi00884a028. [DOI] [PubMed] [Google Scholar]
  14. Stupp Y., Paul W. E., Benacerraf B. Structural control of immunogenicity. 3. Preparation for and elicitation of anamnestic antibody responses by oligo- and poly-lysines and their DNP derivatives. Immunology. 1971 Oct;21(4):595–603. [PMC free article] [PubMed] [Google Scholar]
  15. Taub R. N., Krantz A. R., Dresser D. W. The effect of localized injection of adjuvant material on the draining lymph node. I. Histology. Immunology. 1970 Feb;18(2):171–186. [PMC free article] [PubMed] [Google Scholar]

Articles from Immunology are provided here courtesy of British Society for Immunology

RESOURCES