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1 Metastatic melanoma Primary melanoma Healthy human skin Supplementary Figure 1 CD22 IgG4 Supplementary Figure 1: Immunohisochemical analysis of CD22+ (left) and IgG4 (right), cells (shown in red and indicated by arrows) in healthy skin, primary and metastatic melanoma lesions. Counterstaining in hematoxylin (blue; Scale bar: 1 μm, magnification 1x).
2 A B K1316 P1861 K1316 P1861 K1316 P1861 K1316 P1861 FR-1 CDR-1 GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTCAGACTCTCCTGTGCAGCCTCTGGATTCACCTTTAGCATCTATGCCATGAGCTGGG FR-2 CDR-2 TCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAACTATTAGTGGTAGTGCTGATAGCACATACTACGCAGACTCCGTGAAGGGCCGCTTCACCATCTCCAGAGA FR-3 CDR-3 CAACTCCAAGAACACGCTGTATTTGCAAATGAACAGCCTGAGAACTGAGGACACGGCTGTGTATTACTGTGCGAAAGGGACACTGGCTACGAAGGGCGGTATGGACGTC FR-4 TGGGGCCAAGGGACCACGGTCACCGTCTCCTCA GCC TCC ACC AAG GGC CCA TCC GTC TTC CCC CTG GCG CCC TGC TCC AGG AGC ACC TCC GAG AGC ACA GCC GCC CTG GGC TGC A S T K G P S V F P L A P C S R S T S E S T A A L G C CTG GTC AAG GAC TAC TTC CCC GAA CCG GTG ACG GTG TCG TGG AAC TCA GGC GCC CTG ACC AGC GGC GTG CAC ACC TTC CCG L V K D Y F P I P V T V S W N S G A L T S G V H T F P GCT GTC CTA CAG TCC TCA GGA CTC TAC TCC CTC AGC AGC GTG GTG ACC GTG CCC TCC AGC AGC TTG GGC ACC CAG ACC TAC A V L Q S S G L Y S L S S V V T V P S S S L G T Q T Y K K - - ATC TGC AAC GTG AAT CAC AAG CCC AGC AAC ACC AAG GTG GAC AAG AGA GTT I C N V N H K P S N T K V D K R V T T Supplementary Figure 2: V H -D-J (A) and alignment of γ4 constant region (B) amplified by RT-PCR from a melanoma patient () indicating that the acquired protein sequence has the highest similarity with IGHG4 (Accession P1861;K1316) analysed using Blast/Uniport ( γ4 Supplementary Figure 2
3 p g /m l p g /m l p g /m l p g /m l Supplementary Figure 3 A V E G F 5 *** IL *** 2 M C P -1 *** 3 IF N n s T u m o r c e lls + T u m o r C e lls + T u m o r C e lls + T u m o r c e lls B Tumour cells with lymphocytes Tumour cells without lymphocytes C C T (to a p p r o p r ia te g e n e ) fr o m c o -c u ltu r e IL - 1 IF N IL - 4 V E G F D Supplementary Figure 3: (A) Cytokines secreted in culture supernatants of B cells and PBMCs stimulated with or without A375 melanoma tumour cells were analysed by Luminex bead array analysis. Titres of VEGF, IL-6 and MCP-1, but not of IFN, were significantly increased in cultures treated with tumour cells (*** P<.1; ns = not significant P>.5, analysed by using Mann-Withney-Utest, n=9). (B) Flow cytometric sorting strategy to isolate A375 tumor cells and PBMCs from co-culture experiments; purified cells were used to examine cytokine expression in Figure 3D and expression of cytokines by PBMC in these cultures is depicted in (C). (D) Flow cytometric sorting strategy to isolate B cells from co-culture experiments described in Figure 3F.
4 Supplementary Figure 4 CD64 CD32 CD16 Isotype Supplementary Figure 4: Immunohistochemical analysis of FcγR distribution was conducted using fresh-frozen sections of human melanoma lesions and visualized using AP (in red). Representative images demonstrate all three families of FcγRs, i.e. FcγRI (CD64), FcγRII (CD32) and FcγRIII (CD16) widely expressed in melanoma lesions. Main images were captured at 1x magnification (scale bars: 1 mm); magnified images were captured at 2x (scale bars: 5 mm).
5 CD3 CD22 CD3 % engrafted human CD45 + cells Supplementary Figure 5 A B Spleen Engraftment 6 CSPG4 specific IgG1/IgG4 4 2 Isotype control C PBS Control IgG CSPG4 IgG1 CSPG4 IgG4 CSPG4 IgG1 CSPG4 IgG4 CD8 CD56 CD14 CD22 CD27 CD27 Supplementary Figure 5: (A) Design of in vivo model in NOD/scid/ IL-2Rγ -/- mice to determine antibody-mediated effector functions. (B) Engraftment of human CD45+ immune cells in mouse spleens, evaluated by flow cytometry showed no significant difference in human CD45 + engraftment across treatment groups. (C) Representative flow cytometric gating strategies to identify immune cell subsets within the human CD45 + mouse CD45 - gates engrafted in mouse spleens.
6 n u m b e r o f P a tie n ts Supplementary Figure D is tr ib u tio n o f p a tie n t c o h o r t 7 5 p e rc e n tile % Ig G 4 /Ig G to ta l Supplementary Figure 6: Patient distribution based on % IgG4\IgGtotal; black dashed line indicates the 75 percentile, used as cut off point for cumulative survival analysis (Figure 8).
7 Supplementary Table 1: Clinical parameters and disease staging of peripheral blood donors used for ex vivo B cell cultures at the time of sampling (Figures 2 and 3). Patient ID Gender Age Stage TNM M282 F 43 IB T2a;N;M M285 M 82 IIA T2b;N;M M286 F 68 IIB T4a;N;M M287 F 62 IIIA T2a;N1a;M M338 M 72 IIIB Tx;N2c;M M385 M 67 IIIC Tx;N3;M M38 M 41 IIB T4a;N;M M381 M 57 IB T1b;N;M M386 F 64 IIIB Tx;N2c;M M394 M 56 IIB T4a;N;M M396 M 73 IIC T4b;N;M M397 F 7 IIB T3b;N;M M41 F 6 IIIA T2a;N1a;M M42 M 5 IIIB Tx;N1b;M M44 F 65 IB T2b;N;M M45 M 51 IIC T4b;N;M M48 F 71 IB T1a;N;M M49 F 78 IIA T3a;N;M M43 F 78 IIC T4b;N;M M433 F 48 IIIB T3b;N2c;M M435 M 45 IB T2a;N;M M437 M 46 IIA T3a;N;M M438 F 62 IIA T2b;N;M M443 M 69 IB T2a;N;M M318 M 6 IB T2a;N;M M32 F 71 IIB T3b;N;M M247 F 37 IV T3b;N;M1c M224 F 76 IIB T3b;N;M M223 M 35 IB T2a;N;M
Supplementary Table 3. 3 UTR primer sequences. Primer sequences used to amplify and clone the 3 UTR of each indicated gene are listed.
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Supplementary Document 1. Supplementary Table legends 2. Supplementary Figure legends 3. Supplementary Tables 4. Supplementary Figures 5. Supplementary References 1. Supplementary Table legends Suppl.
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Supplementary Table 1. Sequence of primers for real time PCR. Gene Forward primer Reverse primer S25 5 -GTG GTC CAC ACT ACT CTC TGA GTT TC-3 5 - GAC TTT CCG GCA TCC TTC TTC-3 Mafa cds 5 -CTT CAG CAA GGA
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