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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The protocol presents detailed methods for evaluating whether the nanoemulsion ophiopogonin D adjuvant promotes effective cellular immune responses.

Abstract

As a principal ingredient of vaccines, adjuvants can directly induce or enhance the powerful, widespread, innate, and adaptive immune responses associated with antigens. Ophiopogonin D (OP-D), a purified component extracted from the plant Ophiopogon japonicus, has been found to be useful as a vaccine adjuvant. The problems of the low solubility and toxicity of OP-D can be effectively overcome by using a low-energy emulsification method to prepare nanoemulsion ophiopogonin D (NOD). In this article, a series of in vitro protocols for cellular activity evaluation are examined. The cytotoxic effects of L929 were determined using a cell counting kit-8 assay. Then, the secreted cytokine levels and corresponding immune cell numbers after the stimulation and culture of splenocytes from immunized mice were detected by ELISA and ELISpot methods. In addition, the antigen uptake ability in bone marrow-derived dendritic cells (BMDCs), which were isolated from C57BL/6 mice and matured after incubation with GM-CSF plus IL-4, was observed by laser scanning confocal microscopy (CLSM). Importantly, macrophage activation was confirmed by measuring the levels of IL-1β, IL-6, and tumor necrosis factor alpha (TNF-α) cytokines by ELISA kits after coculturing peritoneal macrophages (PMs) from blank mice with the adjuvant for 24 h. It is hoped that this protocol will provide other researchers with direct and effective experimental approaches to evaluate the cellular response efficacies of novel vaccine adjuvants.

Introduction

Vaccines are an important means of preventing and treating infectious and noncommunicable diseases. The appropriate addition of adjuvants and delivery vehicles to vaccine formulations is beneficial for enhancing the immunogenicity of antigens and generating long-lasting immune responses1. In addition to the classical adjuvant alum (aluminum salt), there are six kinds of adjuvants for vaccines that are currently marketed: MF592,3, AS043, AS033, AS013, CpG10184, and Matrix-M5<....

Protocol

All cell experiments were performed in a cell engineering laboratory equipped with basic operating rooms, buffer rooms, sterile culture rooms, and identification and analysis rooms. The working environment and conditions were free from microbial contamination and other harmful factors. The animal experiments were conducted based on the Guidelines for the Care and Use of Laboratory Animals and were approved by the Laboratory Animal Welfare and Ethics Committee of the Third Military Medical University.

Representative Results

The cellular activity evaluation of the adjuvants OP-D and NOD was completed in vitro according to the protocol. L929 fibroblasts are a useful screening model for the in vitro toxicity testing of NOD (Figure 1). The quantification of inflammatory cytokine levels in the spleen can help researchers better understand the immune response (Figure 2). Monitoring CTLs with ELISpot is the gold standard for assessing antigen-specific T-cell immunity in .......

Discussion

Subunit vaccines provide excellent safety but poor immunogenicity. The main strategy to enhance the immunogenicity is to physically adsorb or couple antigens with adjuvants and incorporate them into the drug delivery systems to promote the uptake and presentation by DCs. Natural plant saponins such as quillaia saponin and its derivatives are highly toxic and are not suitable for the development of human vaccines17. Therefore, the study of the toxic effects of vaccines or adjuvants on cells is a ne.......

Acknowledgements

This study was supported by grant No. 2021YFC2302603 of the National Key Research and Development Program of China, grants No. 31670938, 32070924, 82041045, and 32000651 of the National Natural Science Foundation Program of China, grants No. 2014jcyjA0107 and No. 2019jcyjA-msxmx0159 of the Natural Science Foundation Project Program of Chongqing, grant No. CYS21519 of the Postgraduate Research and Innovation Project of Chongqing, grant No. 2020XBK24 of the Army Medical University Special projects, and grant No. 202090031021 of the National Innovation and Entrepreneurship Program for college students.

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Materials

NameCompanyCatalog NumberComments
0.25% Trypsin-EDTA (1x)GIBCO, USA25200056
96-well filter platesMillipore. Billerica, MACLS3922
AlPO4General Chemical Company, USAnull
Automated Cell CounterCountstar, ChinaIC1000
BALB/c mice and C57BL/6 miceBeijing HFK Bioscience Co. Ltdnull
caprylic/capric triglyceride (GTCC)Beijing Fengli Pharmaceutical Co. Ltd., Beijing, Chinanull
CCK-8 kitsDojindo, JapanCK04
Cell Counting PlateCostar, Corning, USACO010101
Cell Sievebiosharp, ChinaBS-70-CS
Centrifuge 5810 REppendorf, Germany 5811000398
DAPISigma-Aldrich, St. Louis, USAD9542
DMEM basic(1x) mediumGIBCO, USAC11885500BT
DSZ5000X Inverted MicroscopeNikon,JapanDSZ5000X
EL-35 (Cremophor-35)Mumbai, Indianull
ELISpot classicAID, GermanyELR06
Fetal Bovine SerumGIBCO, USA10099141C
Full-function Microplate ReaderThermo Fisher Scientific, USAVL0000D2
GFPSigma-Aldrich, St. Louis, USAP42212
GlutamaxInvitrogen, USA35050061
Granulocyte Macrophage Colony-Stimulating FactorGM-CSF, R&D Systems, USA315-03
HEPESInvitrogen, USA15630106
HF 90/240 IncubatorHeal Force, Switzerlandnull
IL-4PeproTech, USA042149
L929 cell lineFENGHUISHENGWU, China NCTC clone 929 (RRID:CVCL_0462)
Laser Scanning Confocal MicroscopyZeiss, GermanyLSM 980
MONTANE 85 PPISEPPIC, FranceL12910
MONTANOX 80 PPISEPPIC, France36372K
Mouse IFN-γ ELISA kitDakewe, China1210002
Mouse IFN-γ precoated ELISPOT kitDakewe, ChinaDKW22-2000-096
Mouse IL-17A ELISA kitDakewe, China1211702
Mouse IL-17A ELISpotPLUS Kitebiosciences, USA3521-4HPW-2
Mouse IL-1β ELISA kitDakewe, China1210122
Mouse IL-6 ELISA kitDakewe, China1210602
Mouse TNF-α ELISA kitDakewe, China1217202
Non-essential amino acids(100x)Invitrogen, USA11140050
Ophiopogonin-DChengdu Purui Technology Co. Ltd945619-74-9
Penicillin-Streptomycin SolutionInvitrogen, USA15070063
PhalloidinSolarbio, ChinaCA1620
Phosphate Buffered SalineZSGB-BIO, ChinaZLI-9062
Red Blood Cell Lysis BufferSolarbio, ChinaR1010
RPMI 1640 mediumHyclone (Life Technology), USASH30809.01
Sodium pyruvate(100 mM)Invitrogen, USA11360070
SqualeneSigma, USAS3626
β- MercaptoethanolInvitrogen, USA21985023

References

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In VitroCellular ActivityNanoemulsionVaccine AdjuvantOphiopogonin DCellular ResponseAdjuvant EvaluationL929 CellsDMEMCentrifugationMouse SpleenRed Blood Cell LysisCellular Delivery

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