Small-molecular compounds enhance the loading of APC with encephalitogenic MBP protein.

Small-molecular compounds with hydrogen bond (H-bond) donor function are able to trigger exchange reactions of MHC class II ligands. Here, we show that their effect is not limited to short peptides. Also encephalitogenic myelin basic protein (MBP) is transferred with great efficiency onto HLA-DR molecules when H-bond donor molecules such as parachlorphenol (pCP) are present. The effect was observed not only with soluble MHC class II but also with HLA-DR1 and HLA-DR2 molecules on the cell surface. The improved loading of APC translates directly into improved T cell activation. In the presence of pCP T cells reacted at significantly lower antigen concentrations, an effect observed with purified MBP protein as well as with crude spinal cord homogenate. The 'accidental' transfer of autoantigens such as MBP onto activated APC might trigger fatal autoimmune reactions and small molecules as catalysts of this process could represent risk factors, which had not been accounted for as yet.

[1]  C Oseroff,et al.  Structural requirements for binding of an immunodominant myelin basic protein peptide to DR2 isotypes and for its recognition by human T cell clones , 1994, The Journal of experimental medicine.

[2]  L. Santambrogio,et al.  Abundant empty class II MHC molecules on the surface of immature dendritic cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[3]  H. Erlich,et al.  Molecular analysis of HLA class I and class II antigen loss mutants reveals a homozygous deletion of the DR, DQ, and part of the DP region: implications for class II gene order. , 1986, Human immunology.

[4]  D E Geraghty,et al.  Transfer and expression of three cloned human non-HLA-A,B,C class I major histocompatibility complex genes in mutant lymphoblastoid cells. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[5]  L Steinman,et al.  Multiple Sclerosis: A Coordinated Immunological Attack against Myelin in the Central Nervous System , 1996, Cell.

[6]  S. Hauser,et al.  Characterization of the response to myelin basic protein in a non human primate model for multiple sclerosis , 2001, European journal of immunology.

[7]  E. Unanue,et al.  Distinct antigen MHC class II complexes generated by separate processing pathways. , 1996, The EMBO journal.

[8]  E. Malle,et al.  Quantification and mapping of antigenic determinants of serum amyloid A (SAA) protein utilizing sequence-specific immunoglobulins and Eu3+ as a specific probe for time-resolved fluorometric immunoassay. , 1995, Journal of immunological methods.

[9]  William S. Lane,et al.  Predominant naturally processed peptides bound to HLA-DR1 are derived from MHC-related molecules and are heterogeneous in size , 1992, Nature.

[10]  J. Woody,et al.  Human T-cell clones recognize chemically synthesized peptides of influenza haemagglutinin , 1982, Nature.

[11]  P. Ricciardi-Castagnoli,et al.  Developmental plasticity of CNS microglia , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[12]  T. Dyrberg,et al.  Molecular mimicry between non-self, modified self and self in autoimmunity. , 1998, Seminars in immunology.

[13]  N. Letvin,et al.  Active and passively induced experimental autoimmune encephalomyelitis in common marmosets: A new model for multiple sclerosis , 1995, Annals of neurology.

[14]  Don C. Wiley,et al.  Crystal Structure of HLA-DR2 (DRA*0101, DRB1*1501) Complexed with a Peptide from Human Myelin Basic Protein , 1998, The Journal of experimental medicine.

[15]  Eric O Long,et al.  Antigen presentation mediated by recycling of surface HLA-DR molecules , 1995, Nature.

[16]  L. Fugger,et al.  A humanized model for multiple sclerosis using HLA-DR2 and a human T-cell receptor , 1999, Nature Genetics.

[17]  J. Strominger,et al.  Ligand Exchange of Major Histocompatibility Complex Class II Proteins Is Triggered by H-bond Donor Groups of Small Molecules* , 2002, The Journal of Biological Chemistry.

[18]  M. Vrljic,et al.  Formation of a highly peptide-receptive state of class II MHC. , 1998, Immunity.

[19]  H. Mcconnell,et al.  Enhancement of peptide antigen presentation by a second peptide. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[20]  D. Zaller,et al.  Mediation by HLA-DM of dissociation of peptides from HLA-DR , 1995, Nature.

[21]  C. Janeway Immunobiology: The Immune System in Health and Disease , 1996 .

[22]  C. Brosnan,et al.  Induction and Suppression of an Autoimmune Disease by Oligomerized T Cell Epitopes , 2000, The Journal of experimental medicine.

[23]  R. Demars,et al.  Homozygous deletions that simultaneously eliminate expressions of class I and class II antigens of EBV-transformed B-lymphoblastoid cells. I. Reduced proliferative responses of autologous and allogeneic T cells to mutant cells that have decreased expression of class II antigens. , 1984, Human immunology.

[24]  R. Zinkernagel,et al.  Dendritic Cells Induce Autoimmune Diabetes and Maintain Disease via De Novo Formation of Local Lymphoid Tissue , 1998, The Journal of experimental medicine.

[25]  L. Santambrogio,et al.  Studies on the mechanisms by which transforming growth factor-beta (TGF-beta) protects against allergic encephalomyelitis. Antagonism between TGF-beta and tumor necrosis factor. , 1993, Journal of immunology.

[26]  R. Merchant,et al.  Presentation of the self antigen myelin basic protein by dendritic cells leads to experimental autoimmune encephalomyelitis. , 1999, Journal of immunology.

[27]  Eric O Long,et al.  HLA‐DR‐restricted presentation of purified myelin basic protein is independent of intracellular processing , 1997, European journal of immunology.

[28]  V. Kuchroo,et al.  High Frequency of Autoreactive Myelin Proteolipid Protein–Specific T Cells in the Periphery of Naive Mice , 2000, The Journal of experimental medicine.

[29]  D. McFarlin,et al.  Immunological aspects of demyelinating diseases. , 1992, Annual review of immunology.

[30]  Lawrence Steinman,et al.  T-cell epitope of the autoantigen myelin basic protein that induces encephalomyelitis , 1986, Nature.