Efficient Generation of Murine Chimeric Antigen Receptor (CAR)-T Cells

Podsumowanie

This protocol streamlines retroviral vector production and murine T cell transduction, facilitating the efficient generation of mouse CAR-T cells.

Streszczenie

Engineered cell therapies utilizing chimeric antigen receptor (CAR)-T cells have achieved remarkable effectiveness in individuals with hematological malignancies and are presently undergoing development for the treatment of diverse solid tumors. So far, the preliminary evaluation of novel CAR-T cell products has predominantly taken place in xenograft tumor models using immunodeficient mice. This approach is chosen to facilitate the successful engraftment of human CAR-T cells in the experimental setting. However, syngeneic mouse models, in which tumors and CAR-T cells are derived from the same mouse strain, allow evaluation of new CAR technologies in the context of a functional immune system and comprehensive tumor microenvironment (TME). The protocol described here aims to streamline the process of mouse CAR-T cell generation by presenting standardized methods for retroviral transduction and ex vivo T cell culture. The methods described in this protocol can be applied to other CAR constructs beyond the ones used in this study to enable routine evaluation of new CAR technologies in immune-competent systems.

Wprowadzenie

Adoptive T cell therapies expressing chimeric antigen receptors (CARs) have revolutionized the field of cancer immunotherapy by harnessing the power of the adaptive immune system to specifically target and eliminate antigen-positive cancer cells¹. While the success of CAR-T cell therapies targeting B cell malignancies has been clinically validated, preclinical studies performed in animal models remain vital for the development of new CARs targeting solid tumors. However, limited clinical efficacy has been demonstrated in solid tumor indications thus far, and it is becoming increasingly apparent that individual preclinical models do not accurately predict the pharmacodynamics and clinical efficacy of a living medicine^2,3. Therefore, investigators have begun to expand the preclinical study of CAR-T cell products to include parallel assessments in xenograft and syngeneic models of human and murine cancers, respectively.

Unlike xenograft models, where human tumors and T cells are engrafted into immunodeficient mice, syngeneic models enable the examination of CAR-T cell responses in the context of a functional immune system. Specifically, immune-competent mice bearing syngeneic tumors provide a system to study the interaction between adoptively transferred T cells and context-specific milieus - including tumor-associated macrophages (TAMs) and regulatory T cells (Tregs) known to suppress T cell function in the tumor microenvironment (TME)^4,5,6. Moreover, syngeneic models offer an additional platform to assess on-target, off-tumor toxicity, and CAR-T cell interaction with host factors that may lead to additional toxicities, including cytokine release syndrome⁷.

Despite these advantages, the number of syngeneic CAR-T cell studies remains limited. Notably, syngeneic models require autologous engineering of CAR-T cells from the same mouse strain and thus present an additional challenge due to the lack of methodology for efficient murine T cell transduction and ex vivo expansion^2,8. This protocol outlines the methods to achieve stable CAR expression through the production of retroviral vectors and optimized T cell transduction. A schematic of the entire process is shown in Figure 1. The use of this approach demonstrates efficient retroviral transduction of murine CAR-T cells and the achievement of high CAR expression without the need for viral concentration through ultracentrifugation. Strategies to change the antigen-specificity of the CAR construct are discussed in addition to the co-expression of additional transgenes.

Protokół

All animal procedures were performed with approval from the Institutional Animal Care and Use Committee (Columbia University, protocols AC-AABQ5551 and AC-AAAZ4470) using 6-8-week-old female BALB/c or CF57BL/6 mice weighing between 20-25 g. The animals were obtained from a commercial source (see Table of Materials). This protocol is structured around the 'days post-activation' of murine T cells, and viral production begins on Day -2. Retrovirus can be stored at -80 °C following initial production, and for future use of this protocol, one may commence with step 2, T cell isolation and activation on Day 0.

1. Retroviral vector production

NOTE: The viral products have been made replication-defective by separation of the packaging genes into two separate plasmids (see Table of Materials), greatly reducing the likelihood of recombination events and inadvertent production of replication-competent virus.

1. Prepare Phoenix Eco cells one day prior to transfection (Day -2 procedure).
   1. Plate approximately 1 x 10⁷ cells in a 15 cm TC-treated plate or T150 culture flask, using 30 mL of culture medium (Phoenix Eco culture medium, as detailed in Table 1).
   2. Incubate overnight at 37 °C. After 18-24 h, the cells should be approximately 70% confluent and uniformly distributed to ensure a high viral yield without overgrowth.
      NOTE: For optimal results, use cells with a low passage and passage them the day before plating for viral production. Do not allow Phoenix Eco cells to overgrow during routine culture.
2. Prepare the transfection mix containing the lipofection and enhancer reagents, pCL-Eco (Gag/Pol), and pMSCV expression plasmid (pMSCV_PGK_mGFP28z) in reduced-serum media (see Table of Materials) (Day -1 procedure).
   NOTE: Co-transfection should be performed at a 1:1 ratio of pMSCV and pCL-Eco.
   1. Prepare Tube A: Dilute 105 µL of the transfection reagent in 3.75 mL of reduced serum medium per 15 cm plate and mix thoroughly by vortexing or pipetting up and down.
   2. Prepare Tube B: Dilute pMSCV expression plasmid (21 µg) and pCL-Eco (21 µg) with 90 µL of enhancer reagent into 3.75 mL of reduced serum medium per 15 cm plate. Mix well by pipetting up and down.
      NOTE: If generating multiple viral products, set up a master mix containing pCL-Eco and the enhancer reagent.
   3. Add Tube A to Tube B and mix thoroughly by pipetting. Incubate for 10-20 min at room temperature, resulting in a total volume of approximately 7.5 mL.
   4. Carefully remove 10 mL of cell culture media from the Phoenix Eco plate(s) and add the entire volume of the transfection mix to the remaining media by tilting the plate and pipetting dropwise. Return cells to a 37 °C incubator.
3. Change the media on transfected Phoenix Eco cells 16-20 h post-transfection (Day 0 procedure).
   1. Pre-warm serum and β-mercaptoethanol (2-ME, see Table of Materials)-free murine T cell medium (mTCM-viral harvest, as listed in Table 1) to 37 °C using a water or bead bath.
   2. Carefully remove the Phoenix Eco culture medium by tilting the plate and placing the pipette tip at the bottom corner, using a vacuum if possible. Avoid over-drying the cells.
   3. Gently add the warmed mTCM-viral harvest medium to the side of the tilted plate by pipetting 30 mL on the slowest setting. Return cells to a 37 °C incubator.
      NOTE: This step can cause Phoenix Eco cells to detach from the plate and reduce viral titers. Pre-warmed media and gentle pipetting will minimize disruption.
4. Harvest the viral supernatant 48 h post-transfection (Day 1 procedure).
   1. Harvest the viral supernatant and filter it through 0.45 µm PVDF filters (see Table of Materials) to remove cells and debris. Aliquot and freeze the virus at -80 °C or proceed directly to Day 1 of step 3 if using fresh virus.
   2. Determine the viral titer (transducing units/mL) by flow cytometry, as previously described⁹. This step is optional.
      1. Determine the viral titer by small-scale transduction of 1 x 10⁵ activated murine T cells in non-tissue culture (TC)-treated 96-well plates, pre-coated with retronectin (see Table of Materials) and loaded with threefold serial dilutions of retroviral supernatant in a final volume of 100 µL of mTCM-viral harvest medium.
         NOTE: See step 2 and step 3 below for detailed instructions on T cell isolation, activation, and transduction.
      2. Determine CAR surface expression 4-5 days post-transduction by flow cytometry.
      3. Calculate the viral titer according to the formula¹⁰: (N x F x D)/V, where N is the number of cells transduced, F is the frequency of CAR-positive cells, D is the dilution factor, and V is the transduction volume in mL to obtain transducing units (TU)/mL.
         NOTE: Viral titer may decrease upon freeze/thaw; therefore, viral titer is ideally determined on frozen and subsequently thawed virus.

2. Murine T cell isolation

1. Isolate and activate murine T cells (Day 0 procedure).
   NOTE: These steps can be performed at room temperature (RT) or 4 °C and should be carried out in a sterile environment.
   1. Harvest the spleen(s) from the mouse strain of interest (e.g., Balb/c, C57BL/6) as previously described¹¹ and obtain a single-cell suspension through mechanical dissociation.
   2. Using the back of a sterile syringe, crush the spleen(s) through a 70-100 µm cell strainer into a 50 mL conical tube.
   3. After setting the syringe aside, wash the strainer with 5 mL of T cell isolation buffer (phosphate-buffered saline, PBS, supplemented with 2% fetal bovine serum, FBS).
   4. Repeat the mashing step and wash the strainer once more with 5 mL of T cell isolation buffer. Bring the final volume to 50 mL with T cell isolation buffer.
   5. Count live cells using a manual hemocytometer or an automatic cell counter by diluting at a 1:20 ratio and then mixing at 1:1 with trypan blue.
   6. Pellet the cells by centrifugation for 10 min at 450 x g, at 4 °C (or RT), and re-suspend spleenocytes at 1 x 10⁸/mL if using the recommended T cell isolation kit (see Table of Materials).
      NOTE: Spleenocytes can be re-strained through a 40-70 µm strainer at this stage to remove clumps.
2. Isolate CD3⁺ T cells by negative selection following the manufacturer's instructions (see Table of Materials). After magnetic separation, transfer the isolate to a 15 mL conical tube and perform a final live cell count.
3. Pellet the isolated T cells by centrifugation for 10 min at 450 x g, at 4 °C (or RT), and re-suspend them at 1 x 10⁶/mL in mTCM-activation medium (Table 1).
4. Activate T cells by adding murine anti-CD3/anti-CD28 monoclonal antibody-coated magnetic beads (see Table of Materials) at a ratio of 25 µL/1 x 10⁶ T cells and 100 U/mL IL-2.
5. Place the cells in an incubator at 37 °C and leave them overnight.
   NOTE: Due to the small size of T cells, a more accurate live T cell count may be achieved by diluting at a 1:10-1:20 ratio and mixing at 1:1 with trypan blue for manual counting using a hemocytometer. Purity may be determined by flow cytometry by staining cells with a fluorescently conjugated αCD3 antibody. Each spleen will yield between 7-10 x 10⁶ T cells depending on the age and strain of the mouse.

3. Murine T cell transduction

1. Prepare plates for transduction (Day 0 procedure).
   1. Pre-coat non-treated sterile 24-well plates with 0.5 mL of human fibronectin transduction enhancer reagent (see Table of Materials) at a final concentration of 20-40 µg/mL by diluting it in sterile PBS and store at 4 °C overnight.
      NOTE: This step may also be performed on Day 1 by coating non-treated 24-well plates with the transduction reagent and incubating them at room temperature for 2 h.
2. Perform T cell transduction (Day 1 procedure).
   1. Prepare the pre-coated plate for transduction. Remove the transduction reagent from each well of the pre-coated 24-well plate and block with an equivalent volume of sterile-filtered PBS + 2% bovine serum albumin (BSA) (0.5 mL) for 30 min at RT.
   2. Wash once with 0.5-1 mL of PBS.
3. Add 0.5-1 mL of neat retrovirus from step 1 or diluted based on viral titer to each pre-coated well and centrifuge for 90 min at 2,000 x g and 32 °C.
4. Add 1 mL of activated T cells to each virally loaded well and centrifuge for 10 min at 450 x g and 32 °C. Return cells to a 37 °C incubator overnight.
5. 24 h post-transduction, remove 1-1.5 mL of cell culture media and replace it with 1-1.5 mL of mTCM-complete and 10 ng/mL of recombinant human IL-7 and IL-15 (see Table of Materials). Return cells to a 37 °C incubator (Day 2 procedure).
   NOTE: During ex vivo culture, 10 ng/mL of cytokines must be added to the culture every 48 h, and T cells should not be diluted beyond 1 x 10⁶/mL.
6. 48 h post-transduction, transfer cells from the transduction plate into a fresh 24-well or 6-well plate and return cells to a 37 °C incubator (Day 3 procedure).
   NOTE: T cell viability may improve by transferring cells on 24 h to 2 days post-transduction, depending on starting T cell viability and viral titer.
7. De-bead the T cells and confirm CAR expression (Day 5-6 procedure).
   1. Thoroughly re-suspend cells to dissociate activated T cells from the αCD3/CD28-coated beads (see Table of Materials) and place the cell suspension on a magnet for 30 s. Transfer the cell suspension to the desired ex vivo culture vessel and return it to a 37 °C incubator.
      NOTE: T cells may be cultured in culture flasks or deep well culture plates. It is recommended to plate a minimum of 5 x 10⁶ T cells in 30 mL of mTCM-complete medium per well in a deep well of a 6-well format plate (see Table of Materials).
   2. Determine CAR expression by flow cytometry⁸.
      NOTE: GFP-CAR expression was determined by incubation with 100 ng/mL of purified GFP. Incorporation of an N-terminal epitope tag will facilitate the detection of alternative CAR constructs.
8. Perform ex vivo culture of CAR-T cells (Day 7-10 procedure).
   1. During ex vivo culture, maintain the cells by removing 50% of the culture medium and replacing it with fresh mTCM-complete + 2x 10 ng/mL of IL-7 and IL-15 every 48 h.
      NOTE: Murine CAR-T cells are ready for use in downstream applications 7 days post-activation and should not be cryopreserved due to poor viability post-thaw.

Wyniki

The protocol described here aims to standardize the process of murine T cell transduction for the generation of mouse CAR-T cells. Figure 1 provides a detailed description of the steps involved. The process begins with the production of retroviral vectors via co-transfection of viral components into Phoenix Eco cells. Figure 2 provides an image of the optimal density of Phoenix Eco cells on the day of transfection. Isolated T cells are then activated 24...

Dyskusje

This protocol describes the steps and reagents necessary for the retroviral transduction of murine T cells to generate CAR-T cells for in vivo studies. Optimizing retroviral transduction conditions achieves robust CAR expression without the need for viral concentration through ultracentrifugation or additional reagents. However, there are multiple modifications that can be applied to this methodology.

While this protocol describes the example generation of a GFP-specific CAR, these me...

Materiały

Name	Company	Catalog Number	Comments
0.45 μm filters	MilliporeSigma	SLHVR33RS
1 mL syringe	Fisher Scientific	14-955-450
1.5 mL microcentrifuge tubes	Fisher Scientific	05-408-135
10 mL syringe	BD	14-823-16E
100 μm strainer	Corning	07-201-432
15 cm TC treated cell culture dishes	ThermoFisher Scientific	130183
15 mL conical tubes	Falcon	14-959-70C
40 μm strainer	Corning	07-201-430
50 mL conical tubes	Falcon	14-959-49A
70 μm strainer	Corning	07-201-431
Attune NxT Flow Cytometer	ThermoFisher Scientific
BALB/C, 6-8 week old	Jackson Laboratory	651
B-Mercaptoethanol	Gibco	21985023
Bovine Serum Albumin	GOLDBIO	A-420-500
DMEM Medium	Gibco	11965092
Dulbecco's Phosphate Buffered Saline (PBS), without Calcium and Magnesium	Gibco	14-190-250
DynaMag-2 Magnet	Invitrogen	12-321-D
EasySep Magnet	Stemcell Technologies	18000
EasySep Mouse T cell Isolation Kit	Stemcell Technologies	19851
FACS buffer	BD	BDB554657
Fetal bovine serum (FBS)	Corning	MT35011CV
GlutaMAX	Gibco	35-050-061
G-Rex6	Wilson Wolf	80240M
HEPES Buffer Solution	Gibco	15-630-080
Human recombinant IL-15	Miltenyi Biotec	130-095-765
Human recombinant IL-2	Miltenyi Biotec	130-097-748
Human recombinant IL-7	Miltenyi Biotec	130-095-363
Lipofectamine 3000	Invitrogen	L3000008
MEM Non-Essential Amino Acids Solution	Gibco	11140-050
Mouse Anti-CD3 BV421	Biolegend	100228
Mouse Anti-CD3/CD28 Dynabeads	Gibco	11-453-D
Mouse Anti-CD4 BV605	BD	563151
Mouse Anti-CD44 APC	Biolegend	103011
Mouse Anti-CD62L PE-Cy7	Tonbo	SKU 60-0621-U025
Mouse Anti-CD8 APC-Cy7	Tonbo	SKU 25-0081-U025
Nikon Ti2 with Prime 95B camera	Nikon
Non-treated 24 well plates	CytoOne	CC7672-7524
Opti-MEM	Gibco	31-985-062
pCL-Eco	Addgene	#12371
Penicillin/Streptomycin Solution	Gibco	15-070-063
Phoenix Eco cells	ATCC	CRL-3214
pMDG.2	Addgene	#12259
pMSCV_PGK_GFP28z	N/A	Produced by R.LV.
Purified sfGFP	N/A	Produced by R.LV.
RetroNectin ('transduction reagent')	Takara Bio	T100B
RPMI 1640	Gibco	21875
Serological pipette 10 mL	Fisher Scientific	13-678-11E
Serological pipette 25 mL	Fisher Scientific	13-678-11
Serological pipette 5 mL	Fisher Scientific	13-678-11D
Sodium Pyruvate	Gibco	11-360-070
TC-treated 24 well plates	Corning	08-772-1
Trypan blue	Gibco	15-250-061