Role of high-affinity HLA-DP specific CLIP-derived peptides in beryllium binding to the HLA-DPGlu69 berylliosis-associated molecules and presentation to beryllium-sensitized T cells

Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position β69 (HLA-DPGlu69). This study was designed to clarify the preci...

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Published inImmunology Vol. 128; no. 1pt2; pp. e462 - e470
Main Authors Amicosante, Massimo, Berretta, Floriana, Dweik, Raed, Saltini, Cesare
Format Journal Article
LanguageEnglish
Published Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01.09.2009
Blackwell Publishing Ltd
Blackwell Science Inc
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ISSN0019-2805
1365-2567
1365-2567
DOI10.1111/j.1365-2567.2008.03000.x

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Abstract Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position β69 (HLA-DPGlu69). This study was designed to clarify the precise role of peptides in beryllium binding to the HLA-DP groove's pocket 4 and to identify peptides with higher affinity for pocket 4 that might prevent beryllium presentation and T-cell stimulation. Beryllium/HLA-DP interactions were analysed by the ability of beryllium to compete with CLIP and CLIP-derived peptides to HLA-DPGlu69 soluble molecule. The CLIP-derived low-affinity peptide CLIP-AA, could not outcompete beryllium; while the CLIP-derived high-affinity peptides CLIP-YY, CLIP-QY and CLIP-RF were only marginally influenced by the presence of beryllium in the competition assay. The effect of these CLIP-derived high-affinity peptides on beryllium presentation was determined by measuring interferon-γ (IFN-γ) release upon beryllium stimulation of peripheral blood mononuclear cells obtained from beryllium-hypersensitive subjects. CLIP-YY did inhibit beryllium presentation and T-cell activation, while CLIP-QY and CLIP-RF markedly enhanced the IFN-γ response to beryllium. Anti-HLA-DP monoclonal antibody blocked the beryllium-induced IFN-γ release in the presence of CLIP-QY (88%) and CLIP-RF (76%). A similar effect was observed for CLIP-YY capability to block IFN-γ release by beryllium stimulation in the presence of CLIP-QY (79%) and CLIP-RF (76%). Overall, these data support the proposal that HLA-DP high-affinity peptides might be used as a model for specific berylliosis therapy.
AbstractList Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position β69 (HLA-DPGlu69). This study was designed to clarify the precise role of peptides in beryllium binding to the HLA-DP groove's pocket 4 and to identify peptides with higher affinity for pocket 4 that might prevent beryllium presentation and T-cell stimulation. Beryllium/HLA-DP interactions were analysed by the ability of beryllium to compete with CLIP and CLIP-derived peptides to HLA-DPGlu69 soluble molecule. The CLIP-derived low-affinity peptide CLIP-AA, could not outcompete beryllium; while the CLIP-derived high-affinity peptides CLIP-YY, CLIP-QY and CLIP-RF were only marginally influenced by the presence of beryllium in the competition assay. The effect of these CLIP-derived high-affinity peptides on beryllium presentation was determined by measuring interferon-γ (IFN-γ) release upon beryllium stimulation of peripheral blood mononuclear cells obtained from beryllium-hypersensitive subjects. CLIP-YY did inhibit beryllium presentation and T-cell activation, while CLIP-QY and CLIP-RF markedly enhanced the IFN-γ response to beryllium. Anti-HLA-DP monoclonal antibody blocked the beryllium-induced IFN-γ release in the presence of CLIP-QY (88%) and CLIP-RF (76%). A similar effect was observed for CLIP-YY capability to block IFN-γ release by beryllium stimulation in the presence of CLIP-QY (79%) and CLIP-RF (76%). Overall, these data support the proposal that HLA-DP high-affinity peptides might be used as a model for specific berylliosis therapy.
Summary Berylliosis is driven by the accumulation in the lung of beryllium‐specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position β69 (HLA‐DPGlu69). This study was designed to clarify the precise role of peptides in beryllium binding to the HLA‐DP groove’s pocket 4 and to identify peptides with higher affinity for pocket 4 that might prevent beryllium presentation and T‐cell stimulation. Beryllium/HLA‐DP interactions were analysed by the ability of beryllium to compete with CLIP and CLIP‐derived peptides to HLA‐DPGlu69 soluble molecule. The CLIP‐derived low‐affinity peptide CLIP‐AA, could not outcompete beryllium; while the CLIP‐derived high‐affinity peptides CLIP‐YY, CLIP‐QY and CLIP‐RF were only marginally influenced by the presence of beryllium in the competition assay. The effect of these CLIP‐derived high‐affinity peptides on beryllium presentation was determined by measuring interferon‐γ (IFN‐γ) release upon beryllium stimulation of peripheral blood mononuclear cells obtained from beryllium‐hypersensitive subjects. CLIP‐YY did inhibit beryllium presentation and T‐cell activation, while CLIP‐QY and CLIP‐RF markedly enhanced the IFN‐γ response to beryllium. Anti‐HLA‐DP monoclonal antibody blocked the beryllium‐induced IFN‐γ release in the presence of CLIP‐QY (88%) and CLIP‐RF (76%). A similar effect was observed for CLIP‐YY capability to block IFN‐γ release by beryllium stimulation in the presence of CLIP‐QY (79%) and CLIP‐RF (76%). Overall, these data support the proposal that HLA‐DP high‐affinity peptides might be used as a model for specific berylliosis therapy.
Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position beta69 (HLA-DPGlu69). This study was designed to clarify the precise role of peptides in beryllium binding to the HLA-DP groove's pocket 4 and to identify peptides with higher affinity for pocket 4 that might prevent beryllium presentation and T-cell stimulation. Beryllium/HLA-DP interactions were analysed by the ability of beryllium to compete with CLIP and CLIP-derived peptides to HLA-DPGlu69 soluble molecule. The CLIP-derived low-affinity peptide CLIP-AA, could not outcompete beryllium; while the CLIP-derived high-affinity peptides CLIP-YY, CLIP-QY and CLIP-RF were only marginally influenced by the presence of beryllium in the competition assay. The effect of these CLIP-derived high-affinity peptides on beryllium presentation was determined by measuring interferon-gamma (IFN-gamma) release upon beryllium stimulation of peripheral blood mononuclear cells obtained from beryllium-hypersensitive subjects. CLIP-YY did inhibit beryllium presentation and T-cell activation, while CLIP-QY and CLIP-RF markedly enhanced the IFN-gamma response to beryllium. Anti-HLA-DP monoclonal antibody blocked the beryllium-induced IFN-gamma release in the presence of CLIP-QY (88%) and CLIP-RF (76%). A similar effect was observed for CLIP-YY capability to block IFN-gamma release by beryllium stimulation in the presence of CLIP-QY (79%) and CLIP-RF (76%). Overall, these data support the proposal that HLA-DP high-affinity peptides might be used as a model for specific berylliosis therapy.
Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position beta69 (HLA-DPGlu69). This study was designed to clarify the precise role of peptides in beryllium binding to the HLA-DP groove's pocket 4 and to identify peptides with higher affinity for pocket 4 that might prevent beryllium presentation and T-cell stimulation. Beryllium/HLA-DP interactions were analysed by the ability of beryllium to compete with CLIP and CLIP-derived peptides to HLA-DPGlu69 soluble molecule. The CLIP-derived low-affinity peptide CLIP-AA, could not outcompete beryllium; while the CLIP-derived high-affinity peptides CLIP-YY, CLIP-QY and CLIP-RF were only marginally influenced by the presence of beryllium in the competition assay. The effect of these CLIP-derived high-affinity peptides on beryllium presentation was determined by measuring interferon-gamma (IFN-gamma) release upon beryllium stimulation of peripheral blood mononuclear cells obtained from beryllium-hypersensitive subjects. CLIP-YY did inhibit beryllium presentation and T-cell activation, while CLIP-QY and CLIP-RF markedly enhanced the IFN-gamma response to beryllium. Anti-HLA-DP monoclonal antibody blocked the beryllium-induced IFN-gamma release in the presence of CLIP-QY (88%) and CLIP-RF (76%). A similar effect was observed for CLIP-YY capability to block IFN-gamma release by beryllium stimulation in the presence of CLIP-QY (79%) and CLIP-RF (76%). Overall, these data support the proposal that HLA-DP high-affinity peptides might be used as a model for specific berylliosis therapy.Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position beta69 (HLA-DPGlu69). This study was designed to clarify the precise role of peptides in beryllium binding to the HLA-DP groove's pocket 4 and to identify peptides with higher affinity for pocket 4 that might prevent beryllium presentation and T-cell stimulation. Beryllium/HLA-DP interactions were analysed by the ability of beryllium to compete with CLIP and CLIP-derived peptides to HLA-DPGlu69 soluble molecule. The CLIP-derived low-affinity peptide CLIP-AA, could not outcompete beryllium; while the CLIP-derived high-affinity peptides CLIP-YY, CLIP-QY and CLIP-RF were only marginally influenced by the presence of beryllium in the competition assay. The effect of these CLIP-derived high-affinity peptides on beryllium presentation was determined by measuring interferon-gamma (IFN-gamma) release upon beryllium stimulation of peripheral blood mononuclear cells obtained from beryllium-hypersensitive subjects. CLIP-YY did inhibit beryllium presentation and T-cell activation, while CLIP-QY and CLIP-RF markedly enhanced the IFN-gamma response to beryllium. Anti-HLA-DP monoclonal antibody blocked the beryllium-induced IFN-gamma release in the presence of CLIP-QY (88%) and CLIP-RF (76%). A similar effect was observed for CLIP-YY capability to block IFN-gamma release by beryllium stimulation in the presence of CLIP-QY (79%) and CLIP-RF (76%). Overall, these data support the proposal that HLA-DP high-affinity peptides might be used as a model for specific berylliosis therapy.
SummaryPlease cite this article in press as: Amicosante M. et al. Role of high-affinity HLA-DP specific CLIP-derived peptides in beryllium binding to the HLA-DPGlu69 berylliosis-associated molecules and presentation to beryllium-sensitized T cells, Immunology (2009)Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented principally by human leucocyte antigen DP molecules carrying a glutamate at position beta 69 (HLA-DPGlu69). This study was designed to clarify the precise role of peptides in beryllium binding to the HLA-DP groove's pocket 4 and to identify peptides with higher affinity for pocket 4 that might prevent beryllium presentation and T-cell stimulation. Beryllium-HLA-DP interactions were analysed by the ability of beryllium to compete with CLIP and CLIP-derived peptides to HLA-DPGlu69 soluble molecule. The CLIP-derived low-affinity peptide CLIP-AA, could not outcompete beryllium; while the CLIP-derived high-affinity peptides CLIP-YY, CLIP-QY and CLIP-RF were only marginally influenced by the presence of beryllium in the competition assay. The effect of these CLIP-derived high-affinity peptides on beryllium presentation was determined by measuring interferon- gamma (IFN- gamma ) release upon beryllium stimulation of peripheral blood mononuclear cells obtained from beryllium-hypersensitive subjects. CLIP-YY did inhibit beryllium presentation and T-cell activation, while CLIP-QY and CLIP-RF markedly enhanced the IFN- gamma response to beryllium. Anti-HLA-DP monoclonal antibody blocked the beryllium-induced IFN- gamma release in the presence of CLIP-QY (88%) and CLIP-RF (76%). A similar effect was observed for CLIP-YY capability to block IFN- gamma release by beryllium stimulation in the presence of CLIP-QY (79%) and CLIP-RF (76%). Overall, these data support the proposal that HLA-DP high-affinity peptides might be used as a model for specific berylliosis therapy.
Author Dweik, Raed
Saltini, Cesare
Berretta, Floriana
Amicosante, Massimo
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16372883 - Expert Rev Vaccines. 2005 Dec;4(6):881-9
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12615898 - J Exp Med. 2003 Mar 3;197(5):567-74
2469014 - N Engl J Med. 1989 Apr 27;320(17):1103-9
11050177 - Proc Natl Acad Sci U S A. 2000 Nov 7;97(23):12717-22
2139099 - J Exp Med. 1990 Apr 1;171(4):1123-40
11423174 - Hum Immunol. 2001 Jul;62(7):686-93
15778396 - J Immunol. 2005 Apr 1;174(7):4316-24
16697706 - Clin Immunol. 2006 Nov;121(2):134-43
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SSID ssj0013055
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Snippet Berylliosis is driven by the accumulation in the lung of beryllium-specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented...
Summary Berylliosis is driven by the accumulation in the lung of beryllium‐specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented...
Berylliosis is driven by the accumulation in the lung of beryllium‐specific T helper type 1 (Th1) cells recognizing beryllium as antigen when presented...
SummaryPlease cite this article in press as: Amicosante M. et al. Role of high-affinity HLA-DP specific CLIP-derived peptides in beryllium binding to the...
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pubmed
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wiley
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SubjectTerms Adult
antigen presentation
Antigens, Differentiation, B-Lymphocyte
Antigens, Differentiation, B-Lymphocyte - immunology
Antigens, Differentiation, B-Lymphocyte - metabolism
Berylliosis
Berylliosis - immunology
Berylliosis - metabolism
beryllium
Beryllium - immunology
Beryllium - metabolism
biosynthesis
chemistry
CLIP
Female
Histocompatibility Antigens Class II
Histocompatibility Antigens Class II - immunology
Histocompatibility Antigens Class II - metabolism
HLA-DP Antigens
HLA-DP Antigens - chemistry
HLA-DP Antigens - immunology
HLA-DP Antigens - metabolism
human leucocyte antigen
human leucocyte antigen-DP
Humans
immunogenetic
immunogenetics
immunology
Interferon-gamma
Interferon-gamma - biosynthesis
Interferon-gamma - immunology
Lymphocyte Activation
Lymphocyte Activation - immunology
Male
metabolism
Middle Aged
Original
peptide-based therapy
T cells
T-lymphocytes
T-Lymphocytes - immunology
T-Lymphocytes - metabolism
Title Role of high-affinity HLA-DP specific CLIP-derived peptides in beryllium binding to the HLA-DPGlu69 berylliosis-associated molecules and presentation to beryllium-sensitized T cells
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1365-2567.2008.03000.x
https://www.ncbi.nlm.nih.gov/pubmed/19191908
https://www.proquest.com/docview/20781657
https://www.proquest.com/docview/46368270
https://www.proquest.com/docview/734042363
https://pubmed.ncbi.nlm.nih.gov/PMC2753961
Volume 128
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