Method Article

Efficient Tonsillar T Follicular Helper Cell Processing and Functional Analysis through High-dimensional Flow Cytometry

DOI:

10.3791/67188

July 11th, 2025

In This Article

Summary

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Here, we present a protocol for collecting and processing tonsil samples, phenotyping using high-dimensional spectral flow cytometry, and conducting unsupervised analysis.

Abstract

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T follicular helper cells (Tfh) are a subset of CD4+ T helper cells that aid in B cell isotype switching, germinal center (GC) formation, somatic hypermutation, and affinity maturation, thereby helping to orchestrate adaptive humoral immune responses in secondary lymphoid tissues during infection, autoimmunity, and vaccination. Understanding the development and function of Tfh cells is crucial for designing effective vaccines and developing targeted treatment strategies for diseases involving this population. Human tonsil cells are accessible mucosal lymphoid organs. They offer a unique opportunity to profile distinct immune populations like Tfh and GC cells, interrogate cell-to-cell interactions, evaluate dynamic cellular functions, and uncover their regulatory mechanisms at the organ level. In addition, in vitro cultures of tonsil cells are straightforward to process and enable the assessment of Tfh cell biology under various conditions. Here, we introduce a protocol for collection, isolation, preservation, and culture of human tonsil cells. We also describe two optimized spectral flow cytometry panels designed for in-depth characterization of Tfh cells. Last, using a phosphatase protein 2A (PP2A) inhibitor treatment as an example, we demonstrate the efficiency and power of unsupervised analyses of high-dimensional flow cytometry data, effectively uncovering treatment-induced differences on a high-dimensional scale.

Introduction

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T follicular helper cells (Tfh) are a distinct subset of CD4+ helper T cells that are essential for the formation and function of germinal centers (GCs) and B cell antibody production. Tfh cells originate from naïve CD4+ T cells through interactions with antigen-presenting cells and the integration of intrinsic and extrinsic factors, including T cell receptor signaling, costimulatory interactions with B cells, cytokines, and chemokines1. Tfh cells express CXCR5 and PD-1, which guide their position within or near the GC. BCL-6 is the master transcription factor critical for Tfh development, maintenance, and function

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Protocol

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The Code of Ethics of the World Medical Association (Declaration of Helsinki) was followed in all the human research in this study. Human tonsil specimens were obtained from patients with adenotonsillar hypertrophy causing sleep disordered breathing or obstructive sleep apnea, sourced from the Division of Pediatric Otolaryngology, Children's National Hospital, Washington, DC, USA. This study received approval from the Institutional Review Board (IRB) at the Children's National Hospital (IRB protocol number 00009806). Informed consent was signed by the parents or guardians of all enrolled participants, and assent was obtained from minor participants aged 7 year....

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Results

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To compare overall cell viability, we cut the tonsil into three similar pieces and processed them using our protocol under three conditions: (1) same-day processing, (2) overnight storage at 4 °C, and (3) overnight storage on ice. The viability among these three conditions was quite similar without any significant difference (Figure 1A). We also assessed the impact of the thawing process on the viability of cells. The dropwise thawing method we used resulted in significantly higher cell viab.......

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Discussion

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In contrast to previous reports that fresh tonsils should be processed within 3 h after surgery19, we found that fresh tonsil samples could retain their viability when stored at 4 °C and processed within 24 h. To optimize cell viability from tonsil tissue upon thawing from liquid nitrogen storage, we adopted the dropwise thawing method recommended in single-cell sequencing, where high cell viability is greatly valued12. This approach allowed for an optimized recovery o.......

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Disclosures

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The authors have no conflicts of interest to disclose.

Acknowledgements

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This research was supported by the Division of Intramural Research of NIAID, NIH.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Machines and instruments
3 mL Plastic SyringeBD309657
96 Well U Bottom PlateThermo Scientific163320
1.2 mL Cryogenic VialsCorning430487
Cell strainer 70 µm NylonFalcon352350
Cell Culture Dish (60 mm)VWR10062-890
CentrifugeThermo ScientificSorvall Legend XTR
Benchmark B2000-2 MyBath 2L Digital Water BathBenchmarkB2000-2
Fine Scissors - SharpF.S.T14060-11
Plastic Instrument CasesF.S.T20830-05
Spectral flow cytometer, AuroraCytek5L 16UV-16V-14B-10YG-8R
Standard Pattern ForcepsF.S.T11000-13
Standard Pattern ForcepsF.S.T11000-20
Vi-cell Blu cell viability analyzer Beckman CoulterC19201
Reagents
0.5 M EDTA pH 8.0Quality Biology351-027-101
2-MercaptoethanolGibco21985-023
ACK lysing bufferGibcoA10492-01
Antibiotic-antimycotic mix (Penicillin-Streptomycin-Amphotericin B Suspension, 100x)Gibco15240-062
Brilliant Stain Buffer Plus (RUO)BD566385
CantharidinSigmaC7632-25MG
Cytofix Fixation BufferBD554655
Dimethyl sulphoxide (DMSO)SigmaD8418-250ml
DNAase IRoche10104159001
Fetal Bovine Serum (FBS)VWR97068-085
FoxP3/Transcription Factor Staining Buffer SeteBioscience00-5523-00
Gentamicin (50 mg/mL)Gibco15750-060
GolgiplugBD555029
GolgiSTOPBD554724
HEPES (1 M)Gibco15630-080
IonomycinSigma I0634-1mg
L-Glutamine (200 mM)Gibco25030-081
MEM NEAA (100x)Gibco11140-050
Paraformaldehyde 16% solution, EM grade (PFA)Electron Microscopy
 Science
15710Dilute with PBS
PBS, pH 7.4Gibco10010072
Penicillin-Streptomycin (10,000 U/mL)Gibco15140-122
Phorbol 12-Myristate 13-Acetate (PMA)SigmaP8139-1mg
Rate-controlled freezing containersMilliporeCorning CoolCell FTS30
RPMI (+L-Glutamine)Gibco11875-085
Sodium Pyruvate (100 mM)Gibco11360-070
True-Stain Monocyte BlockerBioLegend426103
Buffers
Culture medium10% heat-inactivated FBS (VWR),
2 nM glutamine,
0.055 mM 2-mercaptoethanol,
1% penicillin/streptomycin,
1 mM sodium pyruvate,
10 mM HEPES,
1% non-essential amino acids
in RPMI (+L-Glutamine)
FACS buffer2 mM EDTA and 2% heat inactivated FBS in PBS
Freezing medium90% heat-inactivated FBS and 10% DMSO
Thaw bufferWash buffer + 0.1 mg/mL DNaseI
Tonsil mediumRPMI supplemented with 5% heat-inactivated FBS,
10 mM glutamine,
0.05 mg/mL gentamicin,
1% antibiotic-antimycotic mix
 (penicillin, streptomycin, and amphotericin B).
Wash bufferRPMI (+L-Glutamine) supplemented with 10%  heat-inactivated FBS and 10 mM HEPES
Antibodies & other regents for cytokine panel 
Biotin anti-human CD107a (LAMP-1) AntibodyBioLegend3286042 μL in 200 μL complete culture medium per well.
This antibody was added with cells during PMA/ionomycin stimulation.
Live Dead staining100 μL mix per well
LIVE DEAD BlueThermoL23105 1 : 800, 0.125 μL in 100 μL PBS per well. 
Monocyte block50 μL mix per well
Monocyte blocker bufferBioLegend4261035 μL True Stain monocyte blocker and 45 μL FACS buffer per well
Surface antibodies for cytokine panel
Chemokine receptors mixμL/well 
Anti-human CCR6-BV711BioLegend3534361
Anti-human CCR7-BV421BioLegend3532081
Anti-human CXCR3-PE-Cy5BD5511285
Anti-human CXCR5-BV750BD7471111
Brilliant Stain Buffer Plus (RUO)BD56638510
        18 μL mix per well for chemokine receptors;
Add directed to cells with the monocyte block buffer
Other surface antibody mixμL/well 
Anti-human CD103-BUV661BD7499932.5
Anti-human CD14-Spark Blue 550BioLegend3671482.5
Anti-human CD19-Spark NIR 685BioLegend3022702.5
Anti-human CD25-BB515 BD56446710
Anti-human CD27- Super Bright 436Thermo62-0279-425
Anti-human CD3-BV510BioLegend3448282.5
Anti-human CD38 APC-Fire810BioLegend3035501
Anti-human CD4 CF YG584CytekR7-200412.5
Anti-human CD45RA-BUV395BD7403150.6
Anti-human CD56-BUV737BD6127663.5
Anti-human CD57-FITCBioLegend3596041.2
Anti-human CD69-BUV563BD7487641
Anti-human CD8-BUV805BD6128891.2
Anti-human FAS-BB700BD5665420.6
Anti-human HLA-DR APC-Fire 750BioLegend3076582
Anti-human PD1-BV785BioLegend3299291.2
Anti-human-CD45-PerCPThermoMHCD45311.2
Brilliant Stain Buffer Plus (RUO)BD56638510
FACS buffer61
                                    112 μL mix per well for other surface antibodies;
Add directly to the monocyte block buffer (50 μL) and chemokine receptor mix (18 μL, 50+18+112 = 180 μL in total per well)
Intracelluar cytokine antibodies for cytokine panelμL/well 
Anti-human Granzyme B-PEBD5611421
Anti-human IL10-PE-Dazzle 594BioLegend5068121
Anti-human IL17A-BV605BioLegend5123261
Anti-human IL2-BV650BioLegend5003343
Anti-human IL21- Alexa Fluor 647BD56049310
Anti-human IL4-PerCP Cy5.5BD5612341
Anti-human Perforin-APCBioLegend3533122.5
Anti-human TNFa-PE-Cy7BioLegend5029300.1
Anti-IFNγ-Pacific BlueBioLegend5025221
SAv-BUV615BD6130130.25
Brilliant Stain Buffer Plus (RUO)BD56638510
1x permeabilization buffer eBioscience00-5523-0019.15
       (50 μL mix per well)
Antibodies & other regents for transcription factor panel
CD40 Antibody, anti-humanMiltenyi Biotec130-094-1330.5 μg/mL of culture medium for working concentration
Live Dead staining100 μL mix per well
LIVE DEAD BlueThermoL23105 1 : 800, 0.125 μL in 100 μL PBS per well. 
Monocyte blocker bufferBioLegend4261035 μL True Stain monocyte blocker and 45 μL FACS buffer per well
Surface antibodies for transcription factor panel
Chemokine receptors mixμL/well 
Anti-human CCR6-BV711BioLegend3534361
Anti-human CCR7-BV421BioLegend3532081
Anti-human CXCR5-BV750BD7471111
Brilliant Stain Buffer Plus (RUO)BD56638510
          13 μL mix per well
Other surface antibody mixμL/well 
Anti-human 4-1BB-PE-CY7BioLegend3098182.5
Anti-human CD14-Spark Blue 550BioLegend3671482.5
Anti-human CD19-Spark NIR 685BioLegend3022702.5
Anti-human CD200-PerCP-eFluor 710ThermoFisher46-9200-422.5
Anti-human CD25-PE-Cy5BioLegend3026085
Anti-human CD3-BV510BioLegend3448282.5
Anti-human CD38-APC-Fire810BioLegend3035501
Anti-human CD4-Pacific BlueBioLegend3174231
Anti-human CD40L-PEBD55729915
Anti-human CD45RA-BUV395BD7403150.6
Anti-human CD56-BUV737BD6127663.5
Anti-human CD69-BUV650BioLegend3109342.5
Anti-human CD8-BUV805BD6128891.2
Anti-human HLA-DR APC-Fire 750BioLegend3076582
Anti-human ICOS-BUV563BD7414211.2
Anti-human OX40-APCBioLegend3500085
Anti-human PD1-BV785BioLegend3299291.2
Anti-human-CD45-PerCPThermoMHCD45311.2
Brilliant Stain Buffer Plus (RUO)BD56638510
FACS buffer54.1
               117  μL mix per well for other surface antibodies;
Add directly to the monocyte block  buffer (50 μL) and chemokine receptor mix (13 μL, 50+13+117 = 180 μL in total per well)
Transcription factor antibodies for transcription factor panelμL/well 
Anti-human T-bet-BV605BioLegend6448174
Anti-human Bcl6-PE-CF594BD5624014
Anti-human FoxP3-Alexa Fluor 488BD5608871.6
Anti-human GATA3-BB700BD5666422
Anti-human Ki67-Alexa Fluor 700BD5612770.4
Anti-human Rorgt-Alexa Fluor 647BD5636202
Brilliant Stain Buffer Plus (RUO)BD56638510
1 x Permeabilization buffer eBioscience00-5523-0016
                         40 μL mix per well
Software and Packages for unsupervised analysis
Software/packageVersionSource
1data.table1.16.2The Comprehensive R Archive Network
2FlowJO10.9.0Becton, Dickinson and Company
3pheatmap1.0.12The Comprehensive R Archive Network
4R4.3.2The Comprehensive R Archive Network
5readxl1.4.3The Comprehensive R Archive Network
6Rstudio2023.12.1+402Posit PBC
7Seurat5.1.0The Comprehensive R Archive Network
8SeuratData0.2.2.9001The Comprehensive R Archive Network
9SpectroFlo3.0Cytek
10tidyverse2.0.0The Comprehensive R Archive Network
11viridis0.6.5The Comprehensive R Archive Network

References

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  1. Crotty, S. T follicular helper cell biology: A decade of discovery and diseases. Immunity. 50 (5), 1132-1148 (2019).
  2. Choi, J., et al. Bcl-6 is the nexus transcription factor of t follicular helper cells via repressor-of-repressor circuits.....

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Tags

T Follicular HelperTonsil Cell IsolationFlow CytometrySpectral CytometryGerminal Center CellsAdaptive ImmunityIn Vitro CulturePP2A InhibitorCell Interaction AnalysisB Cell Isotype
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