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*
Immunohematology and Blood Transfusion and
Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands
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Abstract |
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 Top Abstract IntroductionMaterials and MethodsResultsDiscussionReferences |
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Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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) to DQB1*0301/DQA1*03 (hereafter
defined as DQ7a), DQB1*0302/DQA1*03 (DQ8), DQB1*0304/DQA1*03 (hereafter
defined as DQ7b), or DQB1*04/DQA1*03 (DQ4), while DRB1*01 (DR1) and *10
(DR10) alleles are linked to DQB1*0501/DQA1*01 (DQ5).
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), collectively referred to as
DQ3 hereafter. The enhancing DRB1 alleles are DRB1*0401 and *0404,
whereas DRB1 alleles such as DRB1*0402, *1301, and 1302, which all
encode the amino acid sequence motif
70DERAA74 in the HV3 region
of the protein, are dominantly protective (6). Consistent with this model, DQ8 transgenic mice, but not DQ6 (DQB1*0601/DQA1*0103) transgenic mice, develop collagen-induced arthritis (7). The DQ3-DR4 haplotypes have a stronger association with RA and predispose to a more severe disease than the DQ5-DR1 and DQ5-DR10 haplotypes (8, 9). Particularly, individuals with two doses of RA-predisposing DQ3 are significantly more predisposed to RA than individuals with two doses of shared epitope (9). Shared epitope-negative DQ9-DR9 homozygous individuals are predisposed to RA (10), and DQ9-DR9 increases the risk of developing disease in DQ3- and DQ5-heterozygous individuals (9). Noticeably DRB1*0402 with the motif DERAA is the only DR4 allele clearly not associated with RA (11). Moreover, DRB1*1301 and *1302 have a dominant protective effect on disease predisposition over DQ5 (9) and on disease severity over both DQ3 and DQ5 (12).
The mechanism of the DERAA-related protection may involve the
presentation of DRB1-derived peptides by DQ leading either to the
deletion of potential autoreactive T cells in the thymus or to the
generation of DRB1-specific, DQ-restricted immunoregulatory
CD4+ T cells. In various murine autoimmune
disease models, CD4+ T cell responses to self-MHC
Ags have been related to suppression of the disease (13, 14). In addition, MHC-derived peptides constitute a large
fraction of the natural ligands eluted from MHC class II molecules
(15). Whether the immunoregulatory
CD4+ T cells arise directly in the thymus or
acquire their regulatory capacity later in the periphery is still
controversial (reviewed in Ref. 16). Their existence and
their mode of action, i.e., by cytokines such as TGF-
, IL-4, and
IL-10 or by cell-cell contact with the APC, are nonetheless becoming
increasingly clear (17, 18, 19, 20). The regulatory T cells may
have the same or a different specificity as the autoaggressive T
lymphocytes, but they will need to home to the autoimmune-targeted site
to fulfill their suppressive role (21).
CD4+ T cells specific for an epitope of an MHC
class II molecule seem well suited for a protective role in autoimmune
diseases involving inflammation, because MHC class II molecules are
always expressed at sites of inflammation.
The existence of protective, DERAA-specific, DQ-restricted T cells in RA requires the natural processing and presentation of the DERAA sequence. The aim of the present study was to test whether the DERAA-positive DRB1 proteins are processed by human APCs, resulting in the presentation of DRB1-derived peptides carrying the DERAA motif in the context of the RA-predisposing DQ molecules. By analyzing the proliferation of DERAA-specific T cell clones (TCC) generated from a DQ8 homozygous individual with DR4 alleles lacking the DERAA motif, we found natural processing and presentation of the DERAA sequence by APC of all individuals carrying a DERAA-positive DRB1 and a DQ3 allele, i.e., DQ7a or DQ8. Our results clearly demonstrate that DRB1 molecules not only act as restriction elements, but can also act as Ags that are processed and generate DQ-restricted epitopes associated with protection against RA.
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Materials and Methods |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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The 15-mer DERAA peptide with the sequence KDILEDERAAVDTYC (boldface intended to emphasize the presence of the DERAA motif in the sequence) was purchased from Neosystem (Strasbourg, France). Its purity was >99%. All other peptides used in this study were synthesized on an automated multiple peptide synthesizer (Syroll, Multisyntech, Germany) and isolated as previously described (22). The purity of the peptides was determined by analytical reverse phase HPLC as previously described (22) and proved to be at least 70% (UV, 214 nm). The integrity of the peptides was determined by mass spectroscopy as previously described (22).
mAbs B8.11.2 specific for HLA-DR (23) and SPVL3 specific for HLA-DQ (24) were provided by Arend Mulder (Leiden University Medical Center, Leiden, The Netherlands). Fluorescent-labeled mAbs used for FACS analysis were purchased from Becton Dickinson (CD4, CD8, CD28, HLA-DR) or from Leinco (St. Louis, MO; HLA-DQ).
cDNA production and nucleotide sequence determination
RNA from the DRB1*0402 homozygous B lymphocyte cell line (BLCL) YAR [IHW9026] (50 x 106 cells) was isolated using RNAzol (Cinna/Biotecx Laboratories, Houston, TX) and reverse transcribed using oligo(dT) and AmpliTaq from Novagen (Madison, WI). Using the DRB1*04-specific primer pair 5'-CCTGTCCTGTTCTCC-3' (starting 18 nucleotides upstream from the ATG start codon) and 5'-TGGAAGAATGAGAGC-3' (starting 85 nucleotides downstream from the TGA stop codon), we amplified a 904-bp cDNA fragment containing the complete coding region of DRB1*0402. PCR products were purified using MicroSpin S-400 HR columns (Amersham Pharmacia Biotech, Roosendaal, The Netherlands).
Sequencing reactions were set up using the Thermo Sequenase core sequencing kit with 7-deaza-dGTP (Amersham Pharmacia Biotech), with 2 pmol of Texas Red 5'-labeled sequencing primers (Isogen Bioscience, Maarsen, The Netherlands). The primer sequences were 5'-GTCCTGTTCTCCAGCAT-3' (F1), 5'-CGGCGAGTCTATCCTG-3' (F2), 5'-AGAATGAGAGCCAAGCG-3' (R1), and 5'-TGCCTGGATAGAAACCAT-3' (R2). Cycle sequencing was performed on a Peltier Thermal Cycler (PTC-200; MJ Research, Waltham, MA), and subsequent electrophoresis on a Vista DNA Sequencer 725 (Amersham Pharmacia Biotech) for 6 h using a 6% Rapidgel-XL (U.S. Biochemical, Cleveland, OH). We determined the nucleotide sequences of two independently amplified PCR products and obtained identical results.
Production and purification of recombinant DRB1*0402 protein
The full-length DRB1*0402 cDNA fragment was inserted into the
expression vector pET28b (Novagen). Using Escherichia coli
XL1-blue (Stratagene, La Jolla, CA) as host strain, DRB1*0402 protein
expression was induced by
isopropyl--D-thio-galactopyranoside. After
overnight culture the cells were harvested and lysed. The inclusion
bodies were purified by repeated washing/centrifugation cycles and
resuspended in phosphate-Tris-buffered 8 M urea, pH 8, to a final
protein concentration of 3 mg/ml. Purity, estimated by
Coomassie-stained SDS-PAGE, was about 90%.
Human cells and HLA typing
All cells used in this study were isolated from heparinized blood (PBMC) from either healthy volunteers or patients visiting the out-patient clinic of the Department of Rheumatology of Leiden University Medical Center. All donors gave their informed consent. HLA typing was performed in Leiden as described previously (9).
Generation of DERAA-specific T cell lines and clones
PBMC from an HLA-DQ8 homozygous donor were cultured at 106 cells/ml in 5 ml of culture medium (IMDM supplemented with 10% human serum) in the presence of 10 µg/ml peptide KDILEDERAAVDTYC (>99% pure). In parallel, monocytes from the same donor were isolated by adherence, and DC were generated using GM-CSF and IL-4, as previously described (25). After 8 days, the surviving T cells (2 x 105/well in 1 ml of culture medium) were restimulated with autologous monocyte-derived DC (5 x 103/well) preincubated with 10 µg/ml of the same peptide. After 11 days of culture the T cells in individual wells were restimulated separately with irradiated (2000 rad), autologous PBMC (5 x 105/well) preincubated with the peptide (second restimulation). After 2 days 10% IL-2-containing medium (Lymphocult-T, Biotest, Serum Institute, Frankfurt, Germany) was added and refreshed every 3–5 days. The resulting T cell lines were harvested 11 days after the last restimulation. Some of the T cells were restimulated with irradiated, peptide-pulsed, autologous PBMC and supplied with IL-2-containing medium as before, and some were tested for their peptide specificity by proliferation assay using irradiated (3000 rad), HLA-DQ-matched PBMC as APC. After the third round of restimulation, peptide-specific T cell lines were frozen. After thawing, the T cells were cloned nonspecifically by limiting dilution (0.3 cells/well) using 105 irradiated (3000 rad) allogeneic feeder cells (pooled PBMC from five donors), 1 µg/ml PHA, and 20U/ml human rIL-2. After in vitro expansion with feeder cells, PHA, and rIL-2, the resulting TCC were frozen and stored in liquid nitrogen.
In vitro lymphocyte proliferation assay
Proliferation of T cells was measured in flat-bottom 96-well plates (Corning-Costar) in triplicate cultures. Viable T cells (104/well) were cultured in 200 µl of culture medium in the presence of irradiated (3000 rad) PBMC from HLA-DR/DQ-typed individuals (5 x 104/well) and synthetic peptide. Cells were cultured for 3 days at 37°C in 5% CO2 and subsequently for another 16–20 h with [3H]thymidine (0.5 µCi/well). 3H incorporation was measured by liquid scintillation counting. Results are expressed as the mean of triplicate cultures. The SD was <20% of the mean value in all results of this study.
Purification of DQ molecules and DQ-peptide binding assay
As a source of DQ8 molecules BLCL BSM [IHW9032] (DQB1*0302/DQA1*0301 DRB1*0401) homozygous for DQ8 was used. Cells were cultured in RPMI 1640 supplemented with 2 mM L-glutamine, 100 U penicillin/100 µg/ml streptomycin solution, and 10% heat-inactivated FCS (all from Life Technologies, Paisley, U.K.). DQ8 molecules were purified from cleared cell lysate by affinity chromatography essentially as described previously for DR (26). The only modification was the exchange of the last chromatography column from one specific for DR to one carrying mAb SPVL-3 that is specific for DQ.
Peptide binding to DQ8 was determined as described previously (27). In short, purified DQ8 molecules were incubated with fluorescent-labeled standard peptide in the presence of protease inhibitors. The standard peptide in this study was fluorescent-labeled Ii p80–103 (LPKPPKPVSKMRMATPLLMQALPM). Peptides for which the DQ binding capacity was to be determined were added to DQ molecules simultaneously with the standard peptide. The DQ-peptide complexes were separated from free peptide by gel filtration, and the fluorescent emission of the complexes was measured as previously described (27). From the amount of MHC-bound fluorescence obtained in the presence of the labeled standard peptide only (A) and the amount of fluorescence obtained in the additional presence of the unlabeled peptide (B), the ability of each peptide to inhibit the binding of the labeled peptide was calculated ((A - B)/A = inhibition factor). The binding capacity of each test peptide to DQ was expressed as the ratio of the inhibition factor of that peptide and the inhibition factor obtained with the unlabeled standard peptide.
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Results |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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The DQ3-DRB1*0401 haplotype is associated with the most severe form of RA, probably because the DRB1*0401 allele enhances the DQ3-associated disease. In contrast, the closely related allele DRB1*0402, which is also in linkage disequilibrium with DQ3, is dominantly protective. At the start of this study, DRB1*0402 was known to differ from DRB1*0401 in the HV3 region and therefore the HV3 region was thought to be associated with protection. However, a complete sequence comparison between DRB1*0401 and *0402, showing all regions potentially associated with protection, was impossible because the region of DRB1*0402 encoding amino acid residues 92–237 had never been sequenced. Therefore, we determined the nucleotide sequence of the complete coding region of DRB1*0402. For the sequence analysis we used cDNA amplified from the DRB1*0402 homozygous BLCL YAR- and DRB1*04-specific primers.
The resulting DRB1*0402 sequence (EMBL nucleotide sequence databank
accession no. AJ245881, IMTG/HLA database submission no. HWS10000777)
differed from the known DRB1*0401 sequence only at the three known
polymorphic positions, which are in the HV3 region, i.e., in codon 67,
L
I, 70, QD, and 71, KE. This result implies that
67ILEDERAA74
is the only candidate region that can explain the protective effect of
DRB1*0402 in RA.
Generation of DERAA-specific, DQ-restricted TCC
As tools for the analysis of the natural processing of the DERAA
peptide, we generated DERAA peptide-specific, DQ-restricted TCC. We
started by subjecting PBMC from a DQ8-homozygous individual carrying
DR4 molecules without a DERAA motif to repeated stimulation with a
synthetic DERAA peptide with the sequence
65KDILEDERAAVDTYC79,
which is present in all but one of the DERAA-positive DRB1 alleles
(DRB1*1103 carries F instead of I at position 67). Despite the fact
that it is generally assumed impossible to generate T cell responses in
vitro from an unprimed individual, we obtained two DERAA
peptide-specific T cell lines. From one of these lines (Tp7.7) a panel
of 28 TCC was generated that were DERAA-specific because their
proliferation in the presence of DERAA-negative, DQ8 APC was fully
dependent on the addition of exogenous DERAA peptide. The results of a
representative TCC are shown in Fig. 1.
Peptide-specific proliferation was completely inhibited by the
DQ-blocking mAb SPVL-3 (Fig. 1), but was unaffected by the DR-blocking
mAb B8.11.2 (data not shown), showing that the 28 DERAA-specific TCC
were DQ restricted. In agreement with their MHC class II restriction
and their resting state, the TCC expressed high levels of CD4, no CD8,
and very little CD28, as determined by Ab staining and flow cytometry
(data not shown). As usual for human TCC, they also expressed high
levels of HLA-DR and intermediate levels of HLA-DQ. In most of the
experiments described below five DERAA-specific TCC were tested, but
because these TCC yielded essentially the same results only those for
TCC Tp7.7–13 are shown.
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Proliferation of the DERAA-specific, DQ-restricted TCC in the
presence of APC from individuals carrying DQ8 and a DERAA-positive DRB1
allele showed that all three DRB1 molecules tested (DRB1*0402, *1301,
and *1302) were processed by human APC and generated a DERAA peptide
that was presented in the context of DQ8 (Fig. 1). The addition of
exogenous DERAA peptide enhanced the proliferation only slightly,
indicating that the natural processing of the endogenous DERAA-positive
DRB1 proteins was efficient. Proliferation was blocked by DQ-specific
mAb SPVL-3, showing that the response of the TCC to the naturally
processed peptide was also restricted to DQ. After testing APC from six
different DQ8-heterozygous, DERAA-positive individuals, we found no
evidence for differences in processing among DQ8-heterozygous
individuals (Fig. 1), as reported for MHC class II heterozygous mice
(28).
Presentation of DERAA peptide restricted to DQ8 and DQ7a
To test which DQ molecules could act as restriction elements, we
tested five selected DERAA-specific TCC, among which were Tp7.7–13,
against a whole panel of APC from DERAA-negative individuals carrying
different DQ alleles with synthetic DERAA peptide or recombinant
DRB1*0402 protein as the Ags. Of the six different DQ molecules tested
(Fig. 2A), only the two
DQA1*03-chain-containing molecules, DQ8 and DQ7a (Table I), could act
as restriction elements for the DERAA-specific TCC. These DQ molecules
presented both the synthetic and the naturally processed DERAA peptide
(derived from recombinant DRB1*0402 protein) to the TCC (Fig. 2A). Surprisingly, the recombinant protein acted as a much
more potent Ag on a molecular basis than the peptide. In our opinion
there are three possible explanations for this observation. 1) Complete
inclusion bodies of the recombinant protein were added to the cultures,
and these are large enough to sink to the bottom of the well, as we
could demonstrate using the Bradford assay to determine protein
concentration. Thus, the effective concentration of the recombinant
protein was increased. 2) Complete inclusion bodies may be taken up by
the APC much more efficiently than peptides. 3) In a complete protein
or in inclusion bodies the epitope is probably more protected from
proteolytic degradation than in a small peptide.
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B) was analyzed using
proliferation of the DERAA-specific TCC, Tp7.7–13, as a read-out.
Again, all APC processed their endogenous DERAA-positive DRB1 molecule
and presented the DERAA peptide in the context of DQ, showing on that
occasion that a fourth DERAA-positive DRB1 allele, DRB1*1103, which
differs from the other DERAA-positive DRB1 alleles at position 67
(IF), also yielded naturally processed DERAA peptide. Reduced efficacy of DQ7a compared with DQ8 in presenting the DERAA peptide to DERAA-specific TCC
To analyze whether DQ7a and DQ8 differed in efficacy to present
the DERAA peptide to the TCC, we made a dose-response curve of
peptide-dependent TCC proliferation for DQ7a and DQ8 carrying APC. We
included APC carrying DQ7b or DQ9 (Table I) in the analysis because
DQ7b and DQ9 are related variants of DQ8 and DQ7a (Table II). Specifically, these four DQ3
molecules carry the same DQ
chain (DQA1*03). However, in the
-chain DQ7a (DQB1*0301) differs from DQ8 (DQB1*0302) at positions
13, 26, 45, and 57; DQ7b (DQB1*0304) at positions 13, 26, and 45; and
DQ9 (DQB1*0303) at position 57. The peptide concentration needed for a
similar level of TCC proliferation proved similar for DQ8- and
DQ7b-expressing APC and 
10-fold higher for DQ7a-expressing APC (Fig. 3). DQ9-expressing APC gave somewhat
unusual results. The APC from all three different DQ9 individuals that
we tested (DQ2/9, DQ6/9, and DQ9/9) induced high background
proliferation of the TCC, resulting in a low stimulation index (SI) for
the DERAA-specific proliferation (SI varied from 3 to 11). However, the
high background proliferation could be blocked by addition of the
DR-specific mAb B8.11.2 (restoring the SI to 150–300), whereas the
DERAA-specific proliferation was blocked by the DQ-specific mAb SPVL-3
and was unaffected by mAb B8.11.2 (data not shown). The combined
proliferation data (Fig. 3) suggest that the impact of the polymorphism
at position 57 is greater than that of the polymorphisms at position
13, 26, and 45.
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Minimal epitope for DQ8 binding and for proliferation of DERAA-specific TCC
Using a panel of truncated and mutated peptides in a competition
binding assay, we determined the minimal DERAA region involved in
binding to DQ8 (Fig. 4). The longest
DERAA peptide tested had a slightly higher affinity for DQ8 than the
standard peptide (Ii p87–101); all truncated and mutated peptides had
lower affinity. The binding results of the truncated peptides indicate
that the 9-mer
68LEDERAAVD76 is the core
epitope for binding to the DQ8 molecule, but that the flanking residues
K65, D66,
I67, and T77 increase the
DQ8 binding capacity of the peptide. The complete lack of binding by
the D76A substituted peptide shows that
the D76 is essential for DQ8 binding and
indicates that it occupies the p9 pocket.
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). The shortest peptide that induced
significant TCC proliferation (SI, >5) with all four APC was the
12-mer peptide
67ILEDERAAVDTY78. The
results with the truncated peptides indicated that
I67 and Y78 contributed
substantially to T cell recognition (Fig. 5), but that
68LEDERAAVD76 was most
likely to occupy the binding groove in all four DQ molecules. In
agreement with the results presented in Fig. 3, DQ9 APC gave high
background proliferation, hampering clear conclusions, but the
proliferation of the TCC with the truncated peptides presented by the
three other DQ3 APC decreased in the order of DQ8>DQ7b>DQ7a.
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Discussion |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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and 2B). This result also indicated that DRB1 polymorphisms in
the regions flanking the DERAA sequence had no influence on the
processing. Even DRB1*1103 yielded correctly processed DERAA peptide
despite a polymorphism at position 67. In contrast to the study by
Moudgil et al. (28) in mice suggesting differences in
processing among heterozygous individuals, we found no differences
among heterozygous individuals in processing of the DERAA sequence,
even though APC from a total of 16 individuals (5 DERAA-negative and 11
DERAA-positive) were tested. In agreement with the binding motif of DQ8 defined by Kwok at al. (29), the DERAA core epitope identified in this study carried a negatively charged residue (D76) at position 9. However, their motif predicts that a negatively charged residue at position 4 as we found (E71) will result in a 10-fold reduction of the binding to DQ8 (29), suggesting an intermediate affinity of the DERAA peptide for DQ8. Nevertheless, in a previous study (27), the DRB1*0402-derived DERAA peptide (65–79) showed a similar affinity for DQ8 as the type I diabetes-associated glutamic acid decarboxylase (GAD65 peptide 250–273) that carries a core epitope for DQ8 binding with a noncharged residue (F256) at position 4 and a negatively charged residue (E261) at position 9 (29).
In support of our hypothesis that the roles of the different DQ3
molecules (containing the DQA1*03-chain; Table I) in RA are similar, we
found that the DERAA peptide could be presented not only by DQ8 but
also by DQ7a, DQ7b, and DQ9. Similarly, others (30) found
presentation by DQ8 and DQ9 of two gluten-derived peptides. However,
molecular modeling of DQ on the known structure of DR1 (31, 32) indicates that the amino acid sequence differences among
DQB1*0301 (DQ7a), DQB1*0302 (DQ8), DQB1*0303 (DQ9), and DQB1*0304
(DQ7b) are located inside pockets 4 and 9 and in a downward loop
outside the region that can combine with a TCR (DQ7a differs from DQ8
in pockets 4 and 9, from DQ7b in pocket 4, and from DQ9 in pocket 9).
The location of the polymorphic residues (inside the pockets) suggests
that the DQ3 molecules have different peptide binding preferences, but
are indiscriminate in the interaction with TCR. In agreement with the
modeling of DQ, binding studies (29) showed different
peptide binding motifs for these DQ molecules. In particular, DQ7a and
DQ9 differ from DQ8 in preferring a noncharged residue such as A at
position 9. In view of these evident differences in peptide binding
preferences among the DQ3 molecules, our TCC proliferation results
(Figs. 3 and 5) are best explained by a difference in the affinity of
the DERAA peptides for the different DQ3 molecules. Nevertheless, both
DQ7a and DQ8 can bind the 15-mer synthetic DERAA sequence and the
naturally processed DERAA peptide well enough to cause strong
proliferation of the DERAA-specific TCC (Figs. 1 and 2).
There is an extensive literature on the distinct stability and peptide affinity of DQ7a, DQ8, and DQ9 (29, 33, 34, 35). These differences have been highlighted to explain the distinct contributions of DQ7, DQ8, and DQ9 to type I diabetes. Indeed, predisposition to type I diabetes is associated with DQ8, but not with DQ7 (36). In contrast with these ideas, our results show that DQ7a, DQ7b, DQ8, and DQ9 are related enough to present common epitopes, such as ILEDERAAVDTY, which is associated with protection against RA. This finding that all four DQ3 molecules can present theDERAA peptide, albeit with different efficacy, suggests that these molecules may also present the same RA-associated peptides to autoaggressive T cells. As a consequence, DQ7a and DQ9 can be expected to make a similar, but weaker, contribution to RA compared with that of DQ8. However, the roles of DQ7a and DQ9 in RA may also be qualitatively different from that of DQ8, as indicated by some epidemiological observations suggesting a primary role for DQ8 in susceptibility to RA and an additive effect of DQ7a and DQ9 when combined with DQ8 (37). Nevertheless, all these observations support some role for DQ7a and DQ9 in susceptibility to RA.
The difference between RA and type I diabetes in the association of
DQ7a with disease predisposition may be explained by factors such as
the nature of the autoantigens involved and the mechanism of the
predisposition. The early age of onset and the very specific nature of
the targeted cells, i.e., pancreatic -cells, suggests a primary role
for T cells in the etiology of type I diabetes. Conversely, the rather
unspecific reactivity of T and B cells in RA, as underscored by the
rheumatoid factor and the indiscriminate destruction of cartilage and
bone, suggests a more indirect role for T cells in this disease.
Therefore, it is conceivable that the differences among DQ7a, DQ8, and
DQ9, which have dramatic consequences for susceptibility to type I
diabetes, may be less important in RA.
In conclusion, our present results provide molecular support for a role of DRB1-derived peptide presented by RA-predisposing DQ molecules in disease modulation of RA. Our investigations open new avenues in understanding the role of T cells in the pathogenesis of RA and other autoimmune diseases.
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Acknowledgments |
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Footnotes |
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2 Address correspondence and reprint requests to Dr. A. Snijders, Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, Albinusdreef 2, Building 1, E3-Q, P.O. Box 9600, 2300 RC Leiden, The Netherlands.
3 Abbreviations used in this paper: RA, rheumatoid arthritis; TCC, T cell clone(s); BLCL, B lymphocyte cell line; SI, stimulation index.
Received for publication November 7, 2000. Accepted for publication February 8, 2001.
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References |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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-chain peptide prevents diabetes in nonobese diabetic mice. J. Immunol. 164:6610. protein dimer, the class II MHC molecule associated with protection from insulin-dependent diabetes mellitus. J. Immunol. 161:6439. gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus. Nature 329:599.[Medline]
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cpm). In the experiment shown, the maximal
response was 21,000 cpm with DQ8/8 APC, 16,000 cpm with DQ6/7b APC,
13,000 cpm with DQ7a/7a APC, and 5,700 cpm with DQ6/9 APC.