Suppression of experimental allergic encephalomyelitis by a synthetic polypeptide

Three random basic copolymers of amino acids were tested for their effect on experimental allergic encephalomyelitis (EAE). One of these copolymers denoted as Cop 1, composed of alanine, glutamic acid, lysine and tyrosine, with a molecular weight of 23 000, showed a marked suppressive effect on the disease. The intravenous administration of Cop 1 in physiological saline, as late as 5 days following the challenge with the disease‐inducing dose of the basic encephalitogenic protein, reduced the clinical incidence of EAE from 64% in the control group to 22%; the histological lesions were also decreased both in prevalence and in severity. The suppressive effect on the disease attained by the synthetic copolymer is of the same order of magnitude as that previously reported for the basic encephalitogen.

[1]  E. Alvord,et al.  Relationships between antibodies and experimental allergic encephalomyelitis. V. Antibodies and delayed hypersensitivity in production and prevention of experimental allergic encephalomyelitis. , 1970, International archives of allergy and applied immunology.

[2]  E. Alvord,et al.  Dissociation of antibody production from disease suppression in the inhibition of allergic encephalomyelitis by myelin basic protein. , 1970, Journal of immunology.

[3]  M. Sela,et al.  Basic encephalitogenic protein: A simplified purification on sulphoethyl‐sephadex , 1970, FEBS letters.

[4]  J. Salk,et al.  Increases in Serum Lactate Dehydrogenase in Experimental Allergic Encephalomyelitis , 1970, Nature.

[5]  J. Salk,et al.  Experimental allergic encephalomyelitis. An encephalitogenic basic protein from bovine myelin. , 1969, Archives of biochemistry and biophysics.

[6]  E. Einstein,et al.  Protective action of the encephalitogen and other basic proteins in experimental allergic encephalomyelitis. , 1968, Immunochemistry.

[7]  P. Carnegie,et al.  Experimental allergic encephalomyelitis. Isolation of basic proteins and polypeptides from central nervous tissue. , 1967, Biochemical Journal.

[8]  E. Einstein,et al.  Basic proteins from the acidic extract of bovine spinal cord: I. Isolation and characterization , 1966 .

[9]  M. Wilchek,et al.  Synthesis of poly‐L‐arginine , 1966 .

[10]  M. Schwartz,et al.  [55] Lactic dehydrogenase (clinical aspects) , 1966 .

[11]  P. Y. Paterson Experimental allergic encephalomyelitis and autoimmune disease. , 1966, Advances in immunology.

[12]  M. Kies CHEMICAL STUDIES ON AN ENCEPHALITOGENIC PROTEIN FROM GUINEA PIG BRAIN , 1965 .

[13]  E. Alvord,et al.  ENCEPHALITOGEN‐INDUCED INHIBITION OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS: PREVENTION, SUPPRESSION AND THERAPY * , 1965, Annals of the New York Academy of Sciences.

[14]  D. A. Yphantis EQUILIBRIUM ULTRACENTRIFUGATION OF DILUTE SOLUTIONS. , 1964, Biochemistry.

[15]  M. Sela,et al.  Synthesis of poly‐L‐lysine and poly‐L‐lysyl albumin via ϵ,N‐trifluoroacetyl‐α,N‐carboxy‐L‐lysine anhydride , 1963 .

[16]  P. Y. Paterson,et al.  EFFECT OF WHOLE BODY X-IRRADIATION ON INDUCTION OF ALLERGIC ENCEPHALOMYELITIS IN RATS. , 1963, Journal of immunology.

[17]  D. Calne,et al.  Suppression of Experimental Allergic Encephalomyelitis by Cytotoxic Drugs , 1963, Nature.

[18]  E. J. Field,et al.  Encephalitogenic Factor in Experimental ‘Allergic’ Encephalomyelitis , 1963, Nature.

[19]  E. Katchalski,et al.  Synthesis, characterization, and acemization of poly-L-serine. , 1963, Biochemistry.

[20]  M. Sela,et al.  Studies on the chemical basis of the antigenicity of proteins. 5. Synthesis, characterization and immunogenicity of some multichain and linear polypeptides containing tyrosine. , 1962, The Biochemical journal.

[21]  C. Anfinsen,et al.  The Reversible Masking of Amino Groups in Ribonuclease and Its Possible Usefulness in the Synthesis of the Protein , 1962 .

[22]  G. Svet-Moldavsky,et al.  Various Types of Acquired Resistance to Experimental ‘Allergic’ Encephalomyelitis , 1959, Nature.

[23]  S. Moore,et al.  Automatic recording apparatus for use in the chromatography of amino acids. , 1958, Federation proceedings.

[24]  G. Svet-Moldavsky,et al.  Acquired Resistance to Experimental Allergic Encephalomyelitis , 1958, Nature.

[25]  M. Sela,et al.  Synthesis and chemical properties of poly-alpha-amino acids. , 1958, Advances in protein chemistry.

[26]  A. Berger,et al.  Poly-L-histidine , 1957 .

[27]  M. A. Stahmann,et al.  Polypeptide formation by reaction of N-carboxy amino acid anhydrides in buffered aqueous solutions. , 1953, The Journal of biological chemistry.

[28]  A. Berger,et al.  Cleavage of N-Carbobenzoxy Groups by dry Hydrogen Bromide and Hydrogen Chloride , 1952 .

[29]  A. Berger,et al.  Poly-L-aspartic Acid , 1951 .

[30]  T. Rivers,et al.  ENCEPHALOMYELITIS ACCOMPANIED BY MYELIN DESTRUCTION EXPERIMENTALLY PRODUCED IN MONKEYS , 1935, The Journal of experimental medicine.

[31]  H. Leuchs Ueber die Glycin‐carbonsäure , 1906 .