83-5980-77 PD-L1, Avelumab Biosimilar 100ug 052015

※お見積書はカートで印刷できます

特徴

  • Avelumab is a human IgG1 monoclonal antibody directed against the immunosuppressive ligand PD-L1 (programmed death-ligand 1) that prevents its interaction with the inhibitory T-cell receptor, PD-1 (programmed cell death protein 1).
  • Upon binding, avelumab promotes T-cell reactivation and restores T-cell-mediated immune response against tumor cells.
  • Avelumab is also the only PD-L1 antibody so far to also induce antibody-dependent cell-mediated cytotoxicity (ADCC) against tumor cells expressing PD-L1.
  • It was first approved by the FDA in March 2017 for the treatment of patients with metastatic MCC (Merkel cell carcinoma) and later for advanced types of renal cell carcinoma and urothelial cancer.
  • Here are some examples of avelumab’s latest research on advanced and metastatic cancer treatments.
  • In one of the latest studies published in Cell, Chew et al.
  • (2020) hypothesized that inhibition of endocytosis may improve the efficiency of immunotherapeutic antibodies on the clinical outcome of advanced cancer patients.
  • Using PCZ, a dynamin inhibitor in combination with avelumab, they significantly improved the therapeutic response in mice with CT26.WT tumors in terms of tumor growth and clearance.
  • Their data in vivo showed that this was due to an increase in avelumab-mediated ADCC and the induction of a potent immune response against tumor cells.
  • In this study, the temporary inhibition of endocytosis increased tumor cell antigen presentation and target availability for immunotherapeutic agents such as cetuximab, trastuzumab, and avelumab.
  • In early 2020, Tafuri et al.
  • performed a meta-analysis on the response rates of patients treated with PD-1 and PD-L1 inhibitors with urothelial carcinoma refractory to standard treatment.
  • The study focused on five FDA-approved antibodies targeting PD-1 or PD-L1: atezolizumab, durvalumab, avelumab, nivolumab, and pembrolizumab.
  • The authors analyzed objective and complete responses, as well as median overall survival and progression-free survival.
  • They measured higher estimated response rates for the selected antibodies than for the “other salvage therapies”.
  • In January 2020, Elbers et al.
  • published the results of a phase-I feasibility trial for advanced-stage head and neck squamous cell carcinoma (HNSCC) patients unfit for cisplatin treatment.
  • The alternative treatment for these patients consists of radiotherapy with cetuximab but the low 5-year overall survival still highlights the need to improve the current therapy strategy.
  • In this study, the authors tested a combination of cetuximab and PD-L1 immune checkpoint blockade with avelumab.
  • They observed transient and manageable immune-related toxicity that did not impact the toxicity of radiotherapy alone.
  • Based on their results, they concluded that the combination treatment was feasible and needed to be tested on a larger scale.
  • At around the same time, another group conducted a meta-analysis with 6,896 participants in 26 different studies to investigate the incidence and potential factors of fatal adverse events associated with the use of PD-L1 inhibitors for the treatment of patients with advanced cancer.
  • The search was performed on PubMed, Embase, and the Cochrane Library and included four PD-L1 inhibitors: atezolizumab, durvalumab, avelumab, and cemiplimab.
  • The overall incidence of fatal adverse events associated with PD-L1 inhibitors was 1.24%.
  • Interestingly, the incidence of fatal adverse events associated with avelumab was lower than that of both atezolizumab and durvalumab.
  • Keywords: PDL1; PD1; immune checkpoints; avelumab; advanced tumors.
  • Applications:Suitable for use in ELISA.
  • Other applications not tested.
  • Recommended Dilution:Optimal dilutions to be determined by the researcher.
  • Storage and Stability:May be stored at 4℃ for short-term only.
  • Aliquot to avoid repeated freezing and thawing.
  • Store at -20℃.
  • Aliquots are stable for 12 months after receipt.
  • For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

仕様

  • Size:100ug
  • 抗体種類:Mab
  • 宿主:human
  • Source Antibody:human
  • Grade:Affinity Purified
  • Purity:Purified by Protein A/G affinity chromatography. Endotoxin: ≤0.75EU/mg (LAL)
  • Form:Supplied as a sterile, no preservative, no pyrogen, clear, colorless to slightly yellow liquid, which contains d-mannitol, glacial acetic acid, polysorbate 20 and sodium hydroxide, the pH range is 5.0-5.6. BSA and Azide free.
  • Specificity:Recognizes human PDL-1. This non-therapeutic antibody uses the same sequence as the therapeutic antibody Avelumab.
  • Isotype:IgG1,l
  • Calc Crossreactivity:Hu
  • この商品は法規制を確認しておりません。(法規制によって販売できない場合もございます)
  • 製品の仕様は予告なく変更になる場合がございます。最新仕様はメーカーホームページをご確認ください。
  • 【試薬に関するお問合せ】
  • アズワン株式会社 試薬・プロセス材料グループ
  • TEL:06-6447-8641
  • FAX:06-6447-8642
  • E-mail:[email protected]
アズワン品番
83-5980-77
型番
052015
入り数
1個
標準価格
145,000円(税抜)
WEB価格
アズワン在庫 [?]
数量

※お気に入り機能はログイン後にご利用いただけます

よくあるご質問

商品のバリエーション (サイズ違い・スペック違い・オプション品など)

商品イメージ アズワン品番 商品名
83-5980-77
PD-L1, Avelumab Biosimilar 100ug
83-5980-78
PD-L1, Avelumab Biosimilar 1mg

よくあるご質問(FAQ)

掲載カタログ情報

掲載カタログ名 掲載ページ

次の商品を登録しました。

商品計:

お買い物を続ける カートを見る