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Table 6 Efficacy and/or immune responses of experimental bacterin vaccines against Mycoplasma hyopneumoniae tested in pigs.

From: Perspectives for improvement of Mycoplasma hyopneumoniae vaccines in pigs

Mycoplasma strain

Adjuvant/carrier

Route

Nb of vaccinations

Challenge infection

Decrease of

Humoral response

CMI responsea

Other/comments

References

Lung lesions

Clinical signs

M. hyopneumoniae numbers

Serum

BALFb

PRIT-5

Micro-encapsulated (oral); Al(OH)3 (IM)

Oral – IM

3

Yes

Yes

  

IgG, IgA

IgA (nose, saliva)

 

Highest humoral responses in oral group

[103]

PRIT-5

Micro-encapsulated (oral); Al(OH)3 (IM)

Oral – IM – IM/oral

3

Yes

Yes

  

IgG, IgA

IgA (nose, saliva)

 

Highest humoral responses in oral/combined groups

Best protection in IM/oral group

[104]

F7.2C c

Lipo_AMP

IM-IM

2

No

   

IgG, no IgA

no IgA

Th1 – no Th17

E: 3/3 – L: 3/3 d

[105]

Lipo_TLR

IM-IM

no Th1 – no Th17

E: 3/3 – L: 3/3

Lipo_DDA:TDB

ID-IM

Th1 – no Th17

E: 2/3 – L: 1/3

SWE_TLR

IM-IM

Th1 – no Th17

E: 3/3 – L: 1/3

PLGA_TLR

IM-IM

No IgG/IgA

no IgA

no Th1 – Th17

E: 0/3 – L: 0/3

F7.2C

Lipo_DDA:TDB

IM-IM

2

Yes

Yes

Yes

Yes

IgG, IgA

IgA

Th1, Th17, CD8 + 

Also reduction of microscopic lung lesions

IgA response only after challenge

Highest efficacy in SWE_TLR group

[106]

SWE_TLR

Th1, Th17, CD8 + 

PLGA_TLR

Th1, no Th17, CD8 + 

  1. IM, Intramuscularly; ID, intradermally.
  2. aCMI responses were tested by stimulation of peripheral blood mononuclear cells (PBMCs).
  3. bBALF bronchoalveolar lavage fluid.
  4. cThe bacterin was formulated with 1) cationic liposomes + STING ligand c-di-AMP (Lipo_AMP), 2) cationic liposomes with TLR ligands targeting TLR1/2, TLR7/8 and TLR9 (Lipo_TLR), 3) cationic liposome formulation with the MINCLE agonist trehalose 6,6-dibehenate DDA:TDB liposomes (Lipo_DDA:TDB), 4) squalene-in-water emulsion with the same TLR ligands (SWE_TLR), 5) microparticle formulation with the same TLR ligands (PLGA_TLR).
  5. dNumber of induced blood transcriptional modules (BTM) by the vaccine group. In total, three early (E) (day 0 to 1) and three late (L) (day 1 to 7) different BTM) were measured: early inflammatory, early IFN type I, early myeloid cell/DC, late cell cycle, late T/NK-cell, late Ig.