Zhu Xuejing, Liu Jian Corning Incorporated

Corning Life Sciences Asia Technology Center Shanghai 201206, China

本文介紹了Corning NK 細胞活化擴增套裝快速擴增NK細胞的使用方法，以及驗證套裝的培養性能。驗證結果表明Corning NK 細胞活化擴增套裝可以用于NK細胞的大量擴增，并且具有高活力和高殺傷能力。Corning NK 細胞活化擴增套裝包含預包被T-75培養瓶，KBM NK活化培養基，KBM NK活化添加劑和KBM NK擴增培養基。前三個特別設計用于NK活化，zui后一個KBM NK擴增培養基于NK細胞擴增。NK活化培養基和擴增培養基生產都是使用高質量試劑和cGMP級的原料。培養基唯二所含蛋白是注射級的血清白蛋白和重組人胰島素。

介紹

自然殺傷細胞（NK）是重要的免疫細胞，能識別并清除腫瘤和病毒感染。體外大量培養NK細胞，滿足過繼性免疫治療所需一向比較困難。據資料，現有的培養方法都是采用擴增培養基搭配細胞因子（IL-2，IL-7，IL-15）的方案，需要研究者自行優化后使用。

Corning NK 細胞活化擴增套裝提供了NK 細胞活化擴增的全套材料和標準操作方法，所得NK細胞擴增能力強，活性和殺傷能力高。研究者無需優化，而且使用步驟十分精簡。本文還和競爭產品比較了NK細胞產量，活力和NK 細胞體外 陽性表達比率和殺傷能力。

材料和方法

健康供體血液使用淋巴細胞分離液分離PBMCs（外周血單個核細胞）。沖洗緩沖液是PBS，培養容器是透氣細胞培養袋。NK 細胞活化擴增的細胞因子是白介素 2（IL-2）。

NK 細胞活化和擴增

1. 熱滅活自體血漿，56°C，30min。離心， 800 xg ， 20 min，去除沉淀。4°C 保存上清血漿，培養備用。

2.至少5倍體積的PBS（不含鈣鎂）清洗PBMCs。室溫離心500xg，10min，收集PBMCs。 PBMCs稀釋到 1 x 106 cells/mL，使用NK活化培養基配比1.8mL NK活化添加劑和10%自體血漿。

3.預包被T-75培養瓶使用前，用PBS（不含鈣鎂）清洗兩次。添加30 mL PBMC懸液到預包被T-75培養瓶，37°C，5% CO2培養。

注意：第六天之前，如果培養基變黃，細胞密度超過2.0 x 10⁶ cells/mL，需要添加新鮮的NK活化培養基配比10%自體血漿，保持細胞密度在在5 x 10⁵到 2.0 x 10⁶ cells/mL之間。

4.培養第六天，培養液離心，適量NK擴增培養基（1000 IU/mL IL-2 和10%自體血漿）重懸細胞，再轉移到T-225培養瓶或透氣細胞培養袋。

5.每隔兩三天，根據細胞擴增狀態，培養體系中添加新鮮的NK擴增培養基（1000 IU/mL IL-2 和10%自體血漿）保持細胞密度在5 x 10⁵到 2.0 x 10⁶ cells/mL之間。

6.細胞總量到達2 x 10⁹ 后收獲細胞用于CCK8 殺傷力和免疫表型檢測。

注意：整個實驗過程中，細胞懸液吹打和培養容器拍打都要輕柔，以避免細胞損傷，保持細胞活性。

免疫表型

收獲細胞表面標記表達評估方法：CD3-CD56+陽性率。

100 μL PBS 加入 1 x 10⁶ 個細胞，CD3 FITC +CD56 PE抗體染色 20min，染色過程 室溫避光。孵育后，PBS 緩沖液清洗細胞，200 μL PBS 重懸，用于流式細胞分析。每個樣本收集1萬個events，再用histogram overlay subtraction method using BD Accuri C6 軟件。

CCK-8 細胞毒性檢測

 K-562 細胞作為靶細胞。1 x 10⁵ cells/mL的K-562 細胞和 5 x 10⁵ cells/mL的效應細胞共培養（96孔培養板三份，終體積200 μL/孔），37°C 過夜。分析前，每孔添加20 μL細胞計數試劑（ Cell Counting Kit-8 solution ，CCK8, Sigma Cat. No. 96992）， 37°C ，5% CO2孵育1 h。數據讀取：SpectraMax® M4 (Molecular Devices) multifunction microplate reader。

結論
Corning® NK細胞活化擴增培養套裝支持NK細胞的快速擴增，NK細胞產量高（約8.6 萬億，擴增290倍），細胞殺傷力強（效應細胞：靶細胞=5:1 下殺傷力77.9%），與競爭產品相比很有優勢。

Corning NK 細胞活化擴增套裝提供了NK 細胞活化擴增的全套材料和標準操作方法。無需優化，而且使用步驟十分精簡。

重慶市華雅干細胞技術有限公司 ，  ：

Zhu Xuejing, Liu Jian Corning Incorporated

Corning Life Sciences Asia Technology Center Shanghai 201206, China

This application note describes the protocol for rapid expansion of NK cells using the Corning NK Expansion kit, as well as tests that validate the use of the kit. The results support the use of the Corning NK Expansion kit by researchers who need high expan- sion capacity, high viability, and high cytotoxicity of NK cells. The Corning NK Expansion kit contains a pre-coated T-75 flask, KBM NK Primary medium, KBM NK Primary supplement, and KBM NK Expansion medium. The first three components are specifically designed for NK cell activation, while the KBM NK Expansion

medium is utilized for NK cell expansion. Both the KBM NK Primary medium and KBM NK Expansion medium are manufactured using high quality reagents and GMP-grade raw materials. The only pro- teins present in the media are injectable levels of serum albumin and recombinant human insulin.

Introduction

Natural killer (NK) cells are crucial immune cells that can recognize and kill tumors and virus infection. It is difficult to obtain the large numbers of NK cells ex vivo that are necessary for adoptive immu- notherapy. Several methods of NK activation/expansion have been reported that use expansion medium plus various cytokines (e.g., IL-2, IL-7, and IL-15). However, these require further optimization by researchers.

The Corning NK Expansion kit provides a complete set of materials and a standard operating procedure to expand NK cells with high expansion capacity, high viability, and high cytotoxicity. Researchers have no need to further optimize it, and the procedure has mini- mal consumables cost. In this application note, we provide com- petitive data, including cell yields, cell viability, and positive NK ratio and cytotoxicity capability in vitro, that compares the Corning NK expansion kit with other commercially available expansion media.

Materials and Methods

Peripheral blood mononuclear cells (PBMCs) were isolated from healthy donor whole blood using lymphocyte separation medium

(Corning Cat. No. 25-072-CI) according to the manufacturer’s instructions. The wash buffer was PBS (Corning Cat. No. 21-040-CV), and the culture vessel was a gas-permeable cell culture media bag (Corning Cat. No. 88-610-20). Interleukin 2 (IL-2, Corning Cat. No. 354043) was used as an in vitro cytokine for NK cell activation and expansion.