LPS-EB VacciGrade™ - Cell culture tested & sterile - TLR4-based Adjuvant

Lipopolysaccharide from E. coli 0111:B4 | Th1 response

SPECIFICATIONS

Specifications

Source
E. coli serotype O111:K58(B4):H-; ATCC 33780; NCTC 9111; Stoke W strain
Target

TLR4

Working concentration

0.1 - 25 µg/mouse

Solubility

Use endotoxin-free physiological water (NaCl 0.9%).

Appearance (form)
Lyophilized
Reconstitution buffer
Endotoxin-free physiological water (provided)
Sterility

Guaranteed sterile

Endotoxin

The endotoxin level is measured using a chromogenic LAL assay and the TLR4 activity is assessed using HEK-Blue™ TLR4 cells.
The absence of other bacterial components (e.g. peptidoglycans and lipoproteins) is confirmed using HEK-Blue™ TLR2 cells.

Applications

Polarization of adaptive immune response, Th1 cellular responses

Quality control

Each lot is released only after meeting predefined biological activity specifications in a cell-based assay.

Additional information

LPS VacciGrade™ is prepared in a laminar flow hood dedicated to LPS.

CONTENTS

Contents

  • Product: 
    LPS-EB VacciGrade™
  • Cat code: 
    vac-3pelps
  • Quantity: 
    5 x 1e6 EU
Includes:

10 ml sterile endotoxin-free physiological water (NaCl 0.9%)

Shipping & Storage

  • Shipping method:  Room temperature
  • Storage:

    • -20°C
    Stability: -20°C for up to 6 months

    Caution:

    • Avoid repeated freeze-thaw cycles

Details

Lipopolysaccharide (LPS) is a natural adjuvant synthesized by gram-negative bacteria and is a potent activator of the immune system. LPS stimulates the immune response through Toll-like receptor 4 (TLR4) [1].

This recognition involves the binding of LPS with lipopolysaccharide-binding protein (LBP) and subsequently with CD14 which physically associates with a complex including TLR4 and MD2 [2]. Formation of the TLR4-centered LPS receptor complex induces the production of proinflammatory cytokines, such as IL-12 and TNF-α, through the MyD88 pathway.
LPS signaling also involves a MyD88-independent cascade that mediates the expression of IFN-inducible genes.

Similar to other TLR-based adjuvants, LPS drives Th1 immunity [3, 4], although in certain circumstances low-dose inhaled LPS can promote Th2 responses [5]. While LPS is a potent adjuvant, its pyrogenic activity has prevented clinical use of LPS in vaccines. Large quantities of LPS induce the overproduction of cytokines causing septic shock [1].
Intramuscular injection with LPS-EB induced the secretion of the proinflammatory cytokines TNF-α and IL-6 and the Th1-type cytokines, IFN- γ and IL-12 [6]. Cellular assays confirmed that LPS-EB is a potent inducer of dendritic cells activation and maturation via a TLR4 signaling pathway [6].

Most LPS preparations on the market are contaminated by other bacterial components, such as lipoproteins, thus activating TLR2 signaling as well as TLR4 signaling. LPS-EB VacciGrade™ only activates the TLR4 pathway.

 

1. Poltorak A. et al., 1998. Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations in Tlr4 gene. Science, 282(5396): 2085-8.
2. Shimazu R. et al., 1999. MD-2, a molecule that confers lipopolysaccharide responsiveness on Toll-like receptor 4. J Exp Med, 189(11):1777-82.
3. Jamalan M. et al., 2011. Effectiveness of Brucella abortus lipopolysaccharide as an adjuvant for tuberculin PPD. Biologicals: journal of the International Association of Biological Standardization. 39(1); 23-28.
4. Barton G.M. & MedzhitovR., 2002. Control of adaptive immune responses by Toll-like receptors. Curr. Opin. Immunol. 14:380.
5. Iwasaki A. & Medzhitov R., 2004. Toll-like receptor control of the adaptive immune responses. Nat Immunol. 5(10):987-95.
6. Han J. et al., 2014. Characterization of the structure and immunostimulatory activity of a vaccine adjuvant, de-o-acylated lipooligosaccharide. PLoS One. 22;9(1):e85838.

DOCUMENTS

Documents

LPS-EB VacciGrade™

Technical Data Sheet

Validation Data Sheet

Safety Data Sheet

Certificate of analysis

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